Chromosome 17
325 well-documented SNPs on chromosome 17, in order of position (GRCh38).
- rs1062923GEMIN4 · 745,827A;Acommon on affy axiom dataTypical
- rs2740348GEMIN4 · 746,695C;Ccommon on affy axiom dataTypical
- rs12603526NXN · 897,353T;Tcommon genotypeTypical
- rs12150338WDR81 · 1,730,810C;Ccommon on affy axiom dataTypical
- rs2070863SERPINF2 · 1,745,208C;Ccommon in clinvarTypical
- rs1057335SERPINF2 · 1,754,359G;Gcommon in clinvarTypical
- rs9913583SERPINF1 · 1,762,036C;Ccommon in complete genomicsTypical
- rs1136287SERPINF1 · 1,769,982T;T3.9x increased risk of wet ARMD in a Taiwanese Chinese populationWorth knowing
- rs6828SERPINF1 · 1,776,708T;Tcommon in clinvarTypical
- rs391300SRR · 2,312,964T;T1.86x risk for gestational diabetesTypical
- rs98915722,525,214C;CNo summary available.Typical
- rs12603284RAP1GAP2 · 2,868,218C;Ccommon in complete genomicsTypical
- rs1076165RAP1GAP2 · 2,870,106G;Gcommon in complete genomicsTypical
- rs12948217ASPA · 3,494,408A;ACanavan disease (predicted); note issue with microarray data thoughVery important
- rs28940279ASPA · 3,499,000C;CCanavan disease (predicted)Very important
- rs222749TRPV1 · 3,592,080G;Gcommon in complete genomicsTypical
- rs161400LOC105371492 · 3,658,102C;Ccommon in clinvarTypical
- rs34210653ALOX15 · 4,632,019A;AReduced risk for nasal polyps and chronic sinusitisWorth knowing
- rs34230287ARRB2 · 4,710,335C;CNo summary available.Typical
- rs2304973CXCL16 · 4,738,927G;Gcommon in complete genomicsTypical
- rs2286672PLD2 · 4,809,322C;Ccommon on affy axiom dataTypical
- rs2243093GP1BA · 4,932,600C;CNo summary available.Important
- rs6065GP1BA · 4,933,086C;Ccommon in complete genomicsTypical
- rs238238ENO3 · 4,953,081A;Acommon in clinvarTypical
- rs6502867NLRP1 · 5,517,008T;TNo summary available.Typical
- rs115799546NLRP1 · 5,558,964T;TMultiple sclerosis/malignant melanoma mutation genotypeVery important
- rs12150220NLRP1 · 5,582,047A;Aslightly increased risk for several autoimmune diseasesTypical
- rs26706605,615,686A;AnormalTypical
- rs12449580AIPL1 · 6,433,927C;Ccommon in clinvarTypical
- rs1509123FBXO39 · 6,780,559C;Ccommon genotypeTypical
- rs312457SLC16A13 · 7,037,074A;Acommon genotypeTypical
- rs117767867SLC16A11 · 7,043,011C;T1.25x risk for type 2 diabetesMinor
- rs140629318ACADVL · 7,221,966A;GCarrier of a (likely) VLCAD mutationImportant
- rs2309689ACADVL · 7,223,865A;GCarrier of a VLCAD deficiency mutationImportant
- rs2302765CHRNB1 · 7,447,656T;Tcommon in clinvarTypical
- rs2302762CHRNB1 · 7,455,542C;CNo summary available.Typical
- rs2302763CHRNB1 · 7,455,958T;Tcommon in clinvarTypical
- rs11078697SENP3 · 7,565,912C;Ccommon genotypeTypical
- rs2075230LOC100996842 · 7,583,790A;Acommon in clinvarTypical
- rs4227MPDU1 · 7,587,859G;Gcommon in clinvarTypical
- rs11653545FXR2 · 7,608,756G;Gcommon genotypeTypical
- rs1799941SHBG · 7,630,105A;ASex Hormone-Binding Globulin levels are 0.4 standard deviations higherMinor
- rs6258SHBG · 7,631,360C;Ccommon in complete genomicsTypical
- rs6259SHBG · 7,633,209A;AnormalTypical
- rs78378222TP53 · 7,668,434G;Tcancer riskImportant
- rs121912664TP53 · 7,670,699C;TLi-Fraumeni Syndrome (predicted)Very important
- rs28934574TP53 · 7,673,776C;GLi-Fraumeni Syndrome (predicted)Very important
- rs28934576TP53 · 7,673,802C;TLi-Fraumeni Syndrome (predicted)Very important
- rs28934577TP53 · 7,674,193A;CLi-Fraumeni Syndrome (predicted)Very important
- rs11540652TP53 · 7,674,220C;TLi-Fraumeni Syndrome (predicted)Very important
- rs28934575TP53 · 7,674,230C;TLi-Fraumeni Syndrome (predicted)Very important
- rs1625895TP53 · 7,674,797T;Tcommon in clinvarTypical
- rs28934578TP53 · 7,675,088T;Tinfo@snpedia.com would like to hear from youVery important
- rs1042522TP53 · 7,676,154G;GLive 3 years longer. Chemotherapy is more effective.Important
- rs1800371TP53 · 7,676,230A;GSlight increase in breast cancer risk for pre-menopausal African womenMinor
- rs1642785TP53 · 7,676,483G;Gcommon in clinvarTypical
- rs8079544TP53 · 7,676,734C;Ccommon genotypeTypical
- rs2287499TP53 · 7,688,850C;Ccommon in clinvarTypical
- rs2287498TP53 · 7,689,242C;Ccommon in clinvarTypical
- rs16956936DNAH2 · 7,730,374C;Ccommon in complete genomicsTypical
- rs8069344GUCY2D · 8,013,961T;Tcommon in clinvarTypical
- rs7221412LOC105376799 · 8,137,696A;AEarly riser. Wakes up 1 hour earlier than those with GG genotype.Worth knowing
- rs3027172PER1 · 8,152,405G;GAssociated with alcohol dependence and increased drinking in response to psychosocial stress.Worth knowing
- rs3027247CTC1 · 8,227,549A;Acommon in clinvarTypical
- rs10521157STX8 · 9,433,053G;GNo summary available.Typical
- rs8069834MYHAS · 10,394,341A;Acommon in clinvarTypical
- rs34693726MYHAS · 10,409,155G;Gcommon in complete genomicsTypical
- rs6503319MYH3 · 10,670,842C;Cnormal risk of malariaTypical
- rs7218761DNAH9 · 11,790,270C;Ccommon genotypeTypical
- rs4792311ELAC2 · 13,011,692A;AIncreased risk of prostate cancerWorth knowing
- rs990080813,159,478G;Gcommon genotypeTypical
- rs8069770HS3ST3A1 · 13,573,849G;Gcommon in complete genomicsTypical
- rs405482313,721,707T;T1.26x higher risk of aggressive form of prostate cancerWorth knowing
- rs3848445LOC107985080 · 14,390,704T;Tcommon genotypeTypical
- rs13422PMP22 · 15,230,858T;Tcommon in clinvarTypical
- rs85926715,922,707A;ANo summary available.Typical
- rs4273077TNFRSF13B · 16,945,825G;G3.57x increased risk of MGUSWorth knowing
- rs1186793417,030,090C;Ccommon in complete genomicsTypical
- rs4646404PEMT · 17,516,885G;Gcommon/normalTypical
- rs2278952PEMT · 17,582,270G;Gcommon/normalTypical
- rs11868035SREBF1 · 17,811,787A;A1.19x increased risk for T2DTypical
- rs2297508SREBF1 · 17,812,003G;GnormalTypical
- rs1889018SREBF1 · 17,831,426G;GnormalTypical
- rs854777MYO15A · 18,143,584T;Tcommon in clinvarTypical
- rs712270LOC105371568 · 18,153,853A;Acommon in clinvarTypical
- rs1979277SHMT1 · 18,328,782G;Gcommon in clinvarTypical
- rs35790011LOC105371578 · 19,560,278G;Gcommon in complete genomicsTypical
- rs2297518NOS2 · 27,769,571A;ANo summary available.Typical
- rs2248814NOS2 · 27,773,295G;Gcommon/normalTypical
- rs4795067NOS2 · 27,779,649G;Gslight increase in risk for psoriatic arthritisMinor
- rs2239907SARM1 · 28,398,728T;Tcommon in clinvarTypical
- rs6505162MIR3184 · 30,117,165A;A0.43x decreased risk for esophageal cancerWorth knowing
- rs3813034SLC6A4 · 30,197,786A;Acommon in clinvarTypical
- rs1042173SLC6A4 · 30,197,993C;CnormalTypical
- rs140701SLC6A4 · 30,211,514T;TIncreased risk for anxiety disordersMinor
- rs140700SLC6A4 · 30,216,371G;GNo summary available.Typical
- rs2020942SLC6A4 · 30,219,896C;Tcommon in complete genomicsTypical
- rs6354SLC6A4 · 30,222,880G;Gcommon in clinvarTypical
- rs2066713SLC6A4 · 30,224,647A;Gcommon in complete genomicsTypical
- rs4251417SLC6A4 · 30,224,840C;CNo summary available.Typical
- rs2020933SLC6A4 · 30,234,737A;ANo summary available.Typical
- rs4795541SLC6A4 · 30,237,299-;-normalTypical
- rs25531SLC6A4 · 30,237,328T;Tshort form of 5-HTTLPR. lower levels of serotonin, slightly less happy, benefits from more supportWorth knowing
- rs1050565BLMH · 30,249,058C;Cif testicular cancer patient, 5x poorer response to bleomycin chemotherapyWorth knowing
- rs9907627NF1 · 31,232,140G;Gcommon in complete genomicsTypical
- rs1024611CCL2 · 34,252,769G;Gincreased risk of exercise induced ischemia, Increased CCL2 levels; increased rate of HIV progressionWorth knowing
- rs1129844CCL11 · 34,285,875A;AUp to 10 year delay in onset of early-onset Alzheimer's (possibly)Worth knowing
- rs12941376PEX12 · 35,576,129A;Acommon on affy axiom dataTypical
- rs1065341CCL5 · 35,871,589T;Tcommon in complete genomicsTypical
- rs2280788CCL5 · 35,880,401G;GNo summary available.Typical
- rs1713806436,831,827G;Gcommon in complete genomicsTypical
- rs11649743LOC105371754 · 37,714,971A;ALower prostate cancer risk?Worth knowing
- rs4430796HNF1B · 37,738,049A;A1.38x increased risk for prostate cancerWorth knowing
- rs7501939HNF1B · 37,741,165C;TNo summary available.Typical
- rs3760511HNF1B · 37,746,322C;CNo summary available.Minor
- rs38286139,584,800C;Ccommon in complete genomicsTypical
- rs4252596ERBB2 · 39,699,581C;Ccommon in clinvarTypical
- rs1136201ERBB2 · 39,723,335A;Acommon in clinvarTypical
- rs28933370ERBB2 · 39,725,125A;Acommon in complete genomicsTypical
- rs1058808ERBB2 · 39,727,784C;Ccommon in clinvarTypical
- rs9303277IKZF3 · 39,820,216T;T1.46x Increased risk of developing primary biliary cirrhosisWorth knowing
- rs1453560ZPBP2 · 39,867,188T;Tcommon in complete genomicsTypical
- rs806917639,900,944A;AnormalTypical
- rs2305480GSDMB · 39,905,943A;G3.5x increase in risk of asthma for Han ChineseWorth knowing
- rs4795400GSDMB · 39,910,767C;CnormalTypical
- rs7216389GSDMB · 39,913,696C;C0.69x lower risk of Childhood Asthma.Worth knowing
- rs3169572ORMDL3 · 39,921,159G;Gcommon in complete genomicsTypical
- rs16965666CASC3 · 40,147,294T;Tcommon in complete genomicsTypical
- rs13706CDC6 · 40,300,899A;ADecreased risk for certain cancersWorth knowing
- rs9904270LOC105371934 · 40,323,579C;Ccommon in complete genomicsTypical
- rs3136687CCR7 · 40,561,644T;Tcommon in complete genomicsTypical
- rs11650915KRT12 · 40,867,144A;GNo summary available.Typical
- rs4796697KRT13 · 41,502,942C;Ccommon in complete genomicsTypical
- rs9891361KRT13 · 41,503,661A;Acommon in complete genomicsTypical
- rs3826550KRT14 · 41,586,555C;Ccommon in clinvarTypical
- rs1126821JUP · 41,755,893T;Tcommon in clinvarTypical
- rs6503691STAT5B · 42,242,072C;CcommonTypical
- rs1053023STAT3 · 42,313,598T;Tcommon in clinvarTypical
- rs1053005STAT3 · 42,313,892T;Tcommon in clinvarTypical
- rs1053004STAT3 · 42,314,074G;Gcommon in clinvarTypical
- rs2306580STAT3 · 42,339,662C;Ccommon in complete genomicsTypical
- rs2071046NAGLU · 42,537,595G;Gcommon in clinvarTypical
- rs86312NAGLU · 42,544,215C;Ccommon in clinvarTypical
- rs598126COASY · 42,564,502A;Acommon in clinvarTypical
- rs1801175G6PC · 42,903,947T;TGlycogen storage disease, type 1AVery important
- rs2229611G6PC · 42,911,449T;Tcommon in clinvarTypical
- rs817632343,043,694G;Gcommon in clinvarTypical
- rs8176318BRCA1 · 43,045,257C;Ccommon in clinvarTypical
- rs41293463BRCA1 · 43,051,071A;TBRCA1 variant considered pathogenic for breast cancerVery important
- rs45553935BRCA1 · 43,057,122G;Gincreased risk for breast cancerWorth knowing
- rs28897696BRCA1 · 43,063,903T;Tcarrier of two copies of BRCA1 variant; likely to be at high risk for breast/ovarian cancerVery important
- rs41293459BRCA1 · 43,063,930A;Gincreased risk for breast cancerWorth knowing
- rs55770810BRCA1 · 43,063,931A;GLikely miscall in Ancestry data; otherwise, BRCA1 variant likely to be pathogenic for breast cancerVery important
- rs1800747BRCA1 · 43,063,952C;TBRCA1 pathogenic mutation associated with breast cancerVery important
- rs1799967BRCA1 · 43,070,958C;Ccommon in clinvarTypical
- rs4986854BRCA1 · 43,071,031T;TNo summary available.Typical
- rs1799966BRCA1 · 43,071,077C;Cvery slightly increased risk for breast cancerWorth knowing
- rs80357389BRCA1 · 43,076,488C;TBRCA1 variant considered pathogenic for breast cancerVery important
- rs8176199BRCA1 · 43,078,507T;Tcommon in clinvarTypical
- rs3737559BRCA1 · 43,082,287G;GNo summary available.Typical
- rs41293455BRCA1 · 43,082,434A;GBRCA1 variant considered pathogenic for breast cancerVery important
- rs8067269BRCA1 · 43,083,782G;Gcommon in clinvarTypical
- rs2070833BRCA1 · 43,090,832G;Gcommon in clinvarTypical
- rs28897686BRCA1 · 43,091,783A;CBRCA1 pathogenic mutation associated with breast cancerVery important
- rs16942BRCA1 · 43,091,983C;Tvery slightly increased breast cancer riskWorth knowing
- rs2227945BRCA1 · 43,092,113C;CNo summary available.Worth knowing
- rs4986852BRCA1 · 43,092,412T;Tpredisposition to breast cancer?Worth knowing
- rs799917BRCA1 · 43,092,919G;Gcommon in clinvarTypical
- rs1800709BRCA1 · 43,093,010A;Apredisposition to breast cancer?Worth knowing
- rs4986850BRCA1 · 43,093,454T;TNo summary available.Worth knowing
- rs1799950BRCA1 · 43,094,464C;Cvery slightly increased breast cancer riskWorth knowing
- rs587782173BRCA1 · 43,104,867A;CBRCA1 variant considered pathogenic for breast cancerVery important
- rs80356847BRCA1 · 43,104,938A;CLikely to be a BRCA1 pathogenic mutation, but uncertainty remainsVery important
- rs28897672BRCA1 · 43,106,487A;Tconsidered a pathogenic BRCA1 breast cancer variantVery important
- rs80357914BRCA1 · 43,124,027-;AGBRCA1 variant considered pathogenic for breast cancerVery important
- rs386833395BRCA1 · 43,124,028-;-185delAG BRCA1 mutation genotypeVery important
- rs796856605BRCA1 · 43,124,030-;CTBRCA1 (breast cancer) 185delAG carrierVery important
- rs80357713BRCA1 · 43,124,030-;AGrare BRCA1 variant, of unclear pathogenicityImportant
- rs80357438BRCA1 · 43,124,032A;TBRCA1 variant considered likely to be pathogenic for ovarian cancer (by ClinVar)Very important
- rs799906NBR2 · 43,126,099T;Tcommon in clinvarTypical
- rs2072081SLC4A1 · 44,250,125G;Gcommon in clinvarTypical
- rs2285644SLC4A1 · 44,251,253G;GDiego blood group Di(a-b+); found in > 99% of Caucasians and BlacksMinor
- rs5036SLC4A1 · 44,261,577C;TMemphis variant of erythrocyte Band 3 glycoproteinWorth knowing
- rs63751243GRN · 44,349,190A;CLikely miscall in both 23andMe and Ancestry data; otherwise, possible frontotemporal dementia mutationImportant
- rs9897526GRN · 44,349,572G;Gcommon in complete genomicsTypical
- rs5848GRN · 44,352,876T;TSomewhat increased (~2 - 3x) dementia riskImportant
- rs5911ITGA2B · 44,375,697C;CBAK platelet-specific alloantigenMinor
- rs2289681GFAP · 44,911,720C;Ccommon in clinvarTypical
- rs1053578ACBD4 · 45,143,918T;TNo summary available.Typical
- rs11012PLEKHM1 · 45,436,075C;Ccommon on affy axiom dataTypical
- rs2942168LINC02210 · 45,637,484C;CNo summary available.Typical
- rs413778CRHR1-IT1-CRHR1 · 45,639,519T;TNo summary available.Typical
- rs393152CRHR1-IT1-CRHR1 · 45,641,777A;AIncreased risk of both PD and ADMinor
- rs4792887CRHR1-IT1-CRHR1 · 45,799,654C;Ccommon in complete genomicsTypical
- rs16940655CRHR1-IT1-CRHR1 · 45,816,520C;CNo summary available.Typical
- rs242939CRHR1-IT1-CRHR1 · 45,818,213T;Tcommon in complete genomicsTypical
- rs242936CRHR1-IT1-CRHR1 · 45,821,843G;Gcommon in complete genomicsTypical
- rs16940665CRHR1-IT1-CRHR1 · 45,830,530T;TNo summary available.Typical
- rs12185268IMP5 · 45,846,317A;Acommon on affy axiom dataTypical
- rs12373124SPPL2C · 45,846,853T;Tcommon/normalTypical
- rs1864325MAPT · 45,900,461C;CNo summary available.Typical
- rs242557MAPT · 45,942,346A;GnormalTypical
- rs1800547MAPT · 45,974,480A;AMAPT H1/H1 diplotypeMinor
- rs12938245MAPT · 45,983,243C;Ccommon in complete genomicsTypical
- rs2258689MAPT · 45,990,016C;CNo summary available.Typical
- rs143624519MAPT · 45,991,484A;Asome increase in risk for neurodegenerative disordersWorth knowing
- rs1052553MAPT · 45,996,523A;Acommon in clinvarTypical
- rs8070723MAPT · 46,003,698G;G~0.05x (thus greatly) reduced risk for developing progressive supranuclear palsyWorth knowing
- rs9468MAPT · 46,024,197T;Tcommon in clinvarTypical
- rs7521MAPT · 46,028,029A;Acommon in clinvarTypical
- rs199533NSF · 46,751,565A;AIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs5918ITGB3 · 47,283,364C;CMI risk, aspirin resistanceWorth knowing
- rs5917ITGB3 · 47,284,587A;ANo summary available.Typical
- rs2317676ITGB3 · 47,310,917A;Acommon in clinvarTypical
- rs3809865ITGB3 · 47,311,220T;Tcommon in clinvarTypical
- rs4794067TBX21 · 47,731,462C;C2.1x risk for Aspirin Induced Asthma. But possibly lower risk of lupus and intractable Graves' disease.Worth knowing
- rs2240017TBX21 · 47,733,553G;Gnot observed (too rare)Typical
- rs2074190TBX21 · 47,733,844G;G2.2x risk for AIATypical
- rs11650354TBX21 · 47,744,726T;T8x risk for allergic asthmaWorth knowing
- rs16947078TBX21 · 47,748,134A;AcommonTypical
- rs17679445PNPO · 47,944,699G;Gcommon on affy axiom dataTypical
- rs9303542SKAP1 · 48,334,138G;G1.2x increased risk for ovarian cancerMinor
- rs12939811HOXB1 · 48,530,596T;TNo summary available.Typical
- rs8844HOXB9 · 48,621,348C;Ccommon genotypeTypical
- rs8556HOXB13 · 48,728,228G;Gcommon in clinvarTypical
- rs138213197HOXB13 · 48,728,343C;TSignificantly higher risk for prostate cancer in menImportant
- rs2303015CALCOCO2 · 48,852,546T;Tcommon genotypeTypical
- rs627386ABI3 · 49,213,433G;Gcommon genotypeTypical
- rs1165049449,267,824A;ASlightly higher prostate cancer riskMinor
- rs7210100ZNF652 · 49,359,387A;ANo summary available.Worth knowing
- rs16948048ZNF652 · 49,363,104A;Acommon/normalTypical
- rs6917PHB · 49,404,181G;Gcommon in complete genomicsTypical
- rs1694820049,488,950G;GNo summary available.Typical
- rs2072446NGFR · 49,510,457C;Ccommon in complete genomicsTypical
- rs2278163DLX3 · 49,995,062G;Gcommon in clinvarTypical
- rs1061237COL1A1 · 50,185,414A;Acommon in clinvarTypical
- rs1800215COL1A1 · 50,188,134T;Tcommon in clinvarTypical
- rs2075559COL1A1 · 50,189,930G;Gcommon in clinvarTypical
- rs17639446COL1A1 · 50,196,542A;Acommon in complete genomicsTypical
- rs67828806COL1A1 · 50,198,177C;TPossible "Oi/eds syndrome" (mild collagen disorder): Feedback WantedImportant
- rs1800012COL1A1 · 50,200,388A;AComplex; possibly lower risk of ACL ruptures, yet higher risk for bone loss and disc diseaseWorth knowing
- rs1107946COL1A1 · 50,203,629C;Ccommon in complete genomicsTypical
- rs6504649XYLT2 · 50,360,095C;Ccommon in clinvarTypical
- rs1776026856,533,930C;Ccommon genotypeTypical
- rs1776029656,538,256T;Tcommon on affy axiom dataTypical
- rs138924661DGKE · 56,848,773A;ANephrotic syndrome type 7Very important
- rs12938916LOC105371839 · 57,788,926G;Gcommon in complete genomicsTypical
- rs8067912LPO · 58,236,543T;Tcommon genotypeTypical
- rs8082134MPO · 58,275,265G;GNo summary available.Typical
- rs2333227MPO · 58,281,401C;CNo summary available.Typical
- rs2643103BCAS3 · 60,709,264G;Gcommon in complete genomicsTypical
- rs7224438BCAS3 · 60,889,177T;Tcommon genotypeTypical
- rs11079454BRIP1 · 61,679,808T;Tcommon in clinvarTypical
- rs7213430BRIP1 · 61,682,813G;Gcommon in clinvarTypical
- rs4986763BRIP1 · 61,683,635A;Acommon in clinvarTypical
- rs4986764BRIP1 · 61,685,986A;Acommon in clinvarTypical
- rs137852986BRIP1 · 61,716,051A;GIncreased cancer risk; ovarian cancer & relatedVery important
- rs587778134BRIP1 · 61,776,458-;TTOvarian cancer susceptibilityVery important
- rs4988345BRIP1 · 61,847,211G;Gcommon in clinvarTypical
- rs4988344BRIP1 · 61,847,251G;Gcommon in clinvarTypical
- rs4968451BRIP1 · 61,849,946C;C2.33x increased risk for meningiomaWorth knowing
- rs12937080BRIP1 · 61,852,376A;ANo summary available.Typical
- rs2048718BRIP1 · 61,863,458C;Ccommon in clinvarTypical
- rs7213516ANAPC16 · 63,474,189A;Ahigher cardiovascular risk in African AmericansTypical
- rs429063,474,767C;CnormalTypical
- rs4309ACE · 63,482,562C;Ccommon in clinvarTypical
- rs1799752ACE · 63,488,529-;-common in clinvarTypical
- rs4343ACE · 63,488,670A;AACE I/I genotypeWorth knowing
- rs4344ACE · 63,489,363A;Afaster responderTypical
- rs4362ACE · 63,496,400T;Tcommon in clinvarTypical
- rs7209435MAP3K3 · 63,635,604T;Tcommon in complete genomicsTypical
- rs11658329LOC101927898 · 63,685,671G;Gcommon in complete genomicsTypical
- rs2070776CD79B · 63,930,138G;GLikely slightly taller - carrier of two alleles for increased heightWorth knowing
- rs28933978PECAM1 · 64,377,836C;CNo summary available.Typical
- rs1140409DDX5 · 64,500,552A;Acommon in complete genomicsTypical
- rs3972219GNA13 · 65,022,415A;Acommon in complete genomicsTypical
- rs12452285RGS9 · 65,193,569C;Ccommon in complete genomicsTypical
- rs8077696RGS9 · 65,196,443C;Ccommon in complete genomicsTypical
- rs8070231RGS9 · 65,198,827A;Acommon in complete genomicsTypical
- rs2292593RGS9 · 65,201,802T;Tcommon in complete genomicsTypical
- rs479095365,230,912A;Acommon in complete genomicsTypical
- rs7591AXIN2 · 65,528,964A;Acommon in clinvarTypical
- rs7224837AXIN2 · 65,532,005A;Acommon in complete genomicsTypical
- rs8081536AXIN2 · 65,538,333C;Ccommon in complete genomicsTypical
- rs2240307AXIN2 · 65,558,189A;Acommon in clinvarTypical
- rs2240308AXIN2 · 65,558,473A;ANo summary available.Typical
- rs1801689APOH · 66,214,462A;Acommon genotypeTypical
- rs666APOH · 66,228,153C;Ccommon in complete genomicsTypical
- rs11867410APOH · 66,231,245T;Tcommon genotypeTypical
- rs1005651PRKCA · 66,441,893A;Acommon in complete genomicsTypical
- rs228883PRKCA · 66,447,877C;Ccommon in complete genomicsTypical
- rs16960228PRKCA · 66,792,709G;Gcommon in clinvarTypical
- rs87341766,825,243C;Ccommon in complete genomicsTypical
- rs8905PRKAR1A · 68,531,661T;Tcommon in clinvarTypical
- rs2366017LINC01483 · 69,854,760G;Gcommon genotypeTypical
- rs1771858670,648,048G;Gcommon on affy axiom dataTypical
- rs1859962CASC17 · 71,112,612G;G1.28x increased risk for prostate cancerWorth knowing
- rs2229989SOX9 · 72,122,794C;Ccommon in clinvarTypical
- rs12943829SLC39A11 · 72,830,265G;Gcommon genotypeTypical
- rs871443ITGB4 · 75,757,422T;Tcommon in clinvarTypical
- rs743554GALK1 · 75,758,167G;GnormalTypical
- rs1135640ACOX1 · 75,953,459G;Gcommon in clinvarTypical
- rs28936679AANAT · 76,469,731A;Gin Japanese, possible delayed sleep phase conditionWorth knowing
- rs8150RHBDF2 · 76,470,935G;Gcommon in clinvarTypical
- rs478940077,001,815G;Gcommon genotypeTypical
- rs3744064SEC14L1 · 77,215,126C;CNo summary available.Typical
- rs990615577,705,615T;Tcommon in complete genomicsTypical
- rs7208422TMC8 · 78,134,494A;Acommon in clinvarTypical
- rs16970849TMC8 · 78,137,827G;Gcommon in complete genomicsTypical
- rs9893818C17orf99 · 78,146,086C;Ccommon in complete genomicsTypical
- rs2071214BIRC5 · 78,223,510A;ANo summary available.Typical
- rs4969168SOCS3 · 78,357,712A;AObesity and/or Insulin resistance associationsWorth knowing
- rs4789939TIMP2 · 78,885,621C;Ccommon in complete genomicsTypical
- rs1042393GAA · 80,105,798A;Acommon in clinvarTypical
- rs1042395GAA · 80,105,870G;Gcommon in clinvarTypical
- rs2278619GAA · 80,109,927A;Acommon in clinvarTypical
- rs28940868GAA · 80,112,922A;Alikely to have Pompe diseaseVery important
- rs1800309GAA · 80,113,242G;Gcommon in clinvarTypical
- rs1126690GAA · 80,117,606G;Gcommon in clinvarTypical
- rs11652075CARD14 · 80,205,094C;Ccommon in clinvarTypical
- rs7503034SGSH · 80,210,594C;TBenign (harmless) variantTypical
- rs7210438BAIAP2 · 81,086,380C;Ccommon/normalTypical
- rs397514693CSNK1D · 82,265,736C;TMorning Lark (very early riser)Very important
- rs104894561CSNK1D · 82,265,743C;TMorning Lark (very early riser)Very important
- rs9303029C17orf62 · 82,450,939C;Ccommon in complete genomicsTypical
No matches.
Source and license
Adapted from SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.