Chromosome 18
133 well-documented SNPs on chromosome 18, in order of position (GRCh38).
- rs3819102ENOSF1 · 675,307A;Acommon in complete genomicsTypical
- rs1826508LOC105371953 · 1,206,983T;Tcommon genotypeTypical
- rs18793522,498,055T;Tcommon on affy axiom dataTypical
- rs643507LPIN2 · 2,946,293T;Tcommon genotypeTypical
- rs8087073LOC105371963 · 2,967,847A;Acommon genotypeTypical
- rs16235233,328,748T;TnormalTypical
- rs543355LAMA1 · 6,958,610T;Tcommon genotypeTypical
- rs16951095LAMA1 · 7,042,912C;Ccommon on affy axiom dataTypical
- rs7243299PTPRM · 7,755,773T;Tcommon in complete genomicsTypical
- rs8098064PTPRM · 8,209,271G;Gcommon in complete genomicsTypical
- rs1156044NDUFV2 · 9,102,142A;Acommon in complete genomicsTypical
- rs906807NDUFV2 · 9,117,869T;Tcommon in clinvarTypical
- rs28645279,288,458T;TNo summary available.Typical
- rs8092502CIDEA · 12,263,374T;Tcommon genotypeTypical
- rs2542151PTPN2 · 12,779,948G;G2x risk for Crohn's; 1.6x for T1DWorth knowing
- rs1893217PTPN2 · 12,809,341G;GSomewhat increased (~2x) risk for Crohn's diseaseWorth knowing
- rs478582PTPN2 · 12,835,977T;Tcommon/normalTypical
- rs7234029PTPN2 · 12,877,061G;GSlightly increased (1.6x) risk for Crohn's diseaseMinor
- rs2186944MC2R · 13,915,543G;Gcommon in complete genomicsTypical
- rs433142622,610,832A;Acommon in complete genomicsTypical
- rs2510344NPC1 · 23,533,321T;Tcommon in clinvarTypical
- rs2236707NPC1 · 23,535,033C;Tcommon in complete genomicsTypical
- rs28942106NPC1 · 23,535,683T;Tcommon in clinvarTypical
- rs1788799NPC1 · 23,544,981C;Ccommon in clinvarTypical
- rs1805081NPC1 · 23,560,468A;GNo summary available.Typical
- rs1154233LAMA3 · 23,931,125A;Acommon in clinvarTypical
- rs11665084HRH4 · 24,476,802C;Ccommon on affy axiom dataTypical
- rs11662595HRH4 · 24,477,006G;GNo summary available.Worth knowing
- rs996683225,825,224A;Acommon genotypeTypical
- rs16942421KCTD1 · 26,576,461G;Gcommon on affy axiom dataTypical
- rs9951307AQP4 · 26,850,565A;AnormalTypical
- rs1694401127,712,399C;Ccommon in complete genomicsTypical
- rs2298574CDH2 · 27,989,094A;Acommon in complete genomicsTypical
- i3002758TTR · 29,172,937A;ATTR-related Familial Amyloid PolyneuropathyVery important
- rs272940930,561,722G;Gcommon in complete genomicsTypical
- rs1426310DSG1 · 31,318,331A;Acommon in clinvarTypical
- rs7236477DSG1 · 31,322,359A;Acommon on affy axiom dataTypical
- rs3752095DSG1-AS1 · 31,354,718A;Acommon in clinvarTypical
- rs4799570DSG1-AS1 · 31,406,370A;Acommon in clinvarTypical
- rs1380866DSG3 · 31,475,994G;Gcommon in complete genomicsTypical
- rs2230234DSG2 · 31,524,751A;Acommon in clinvarTypical
- rs200484060DSG2 · 31,536,370G;GLikely miscall if from Ancestry data; otherwise, ARVC mutationImportant
- rs1800458TTR · 31,592,902G;Gcommon in clinvarTypical
- rs11541790TTR · 31,592,956C;TTTR-related amyloidosisVery important
- rs28933979TTR · 31,592,974A;GTTR-related amyloidosisVery important
- rs121918070TTR · 31,595,157A;GTTR-related amyloidosisVery important
- rs76992529TTR · 31,598,655A;GTTR-related amyloidosisVery important
- rs166725531,607,316A;Adecrease circulating retinol levelsMinor
- rs10438933B4GALT6 · 31,693,166A;ANo summary available.Typical
- rs1050257531,756,628A;Acommon genotypeTypical
- rs17739703CCDC178 · 32,943,324T;Tcommon in complete genomicsTypical
- rs201611635,414,928A;Acommon in complete genomicsTypical
- rs995385235,517,996C;Ccommon genotypeTypical
- rs17647532GALNT1 · 35,654,108C;Creduced risk for ovarian cancer originally reported, but did not replicate in larger studyTypical
- rs76753135,777,904T;Tcommon genotypeTypical
- rs1050631SLC39A6 · 36,114,157A;AMean Survival Time of 17 months for esophageal squamous-cell carcinomaWorth knowing
- rs17651157FHOD3 · 36,527,489T;Tcommon in complete genomicsTypical
- rs1697505041,607,206T;Tcommon genotypeTypical
- rs995803241,648,346C;Ccommon genotypeTypical
- rs16976171LINC00907 · 42,479,656G;Gcommon genotypeTypical
- rs16977065RIT2 · 42,857,686C;Ccommon in complete genomicsTypical
- rs998124LOC105372091 · 45,145,697A;Acommon in complete genomicsTypical
- rs8085664SLC14A2 · 45,234,191A;A0.61x reduced risk of Male Pattern Baldness.Worth knowing
- rs10502868SLC14A2 · 45,573,984T;Tcommon in complete genomicsTypical
- rs1058396LOC105372093 · 45,739,554A;AJk(a-/b+) Kidd blood group, barring other variantsMinor
- rs17859515SLC14A1 · 45,739,554G;GNo summary available.Typical
- rs1450425LOXHD1 · 46,529,070C;Tbenign most likelyTypical
- rs809140647,737,664A;Acommon in complete genomicsTypical
- rs4939827SMAD7 · 48,927,093T;T1x risk for colorectal cancerMinor
- rs12953717SMAD7 · 48,927,559C;C1.37x increased risk for colorectal cancerTypical
- rs4464148SMAD7 · 48,932,662C;C1.35x increased risk for colorectal cancerWorth knowing
- rs736839SMAD7 · 49,001,695C;Ccommon, increased risk for sickle cell leg ulcersTypical
- rs7241918LOC105372112 · 49,634,583T;Tcommon on affy axiom dataTypical
- rs4939883LOC105372112 · 49,640,844C;Cassociated with higher HDL cholesterolMinor
- rs2156552LOC105372112 · 49,655,298T;Tcommon on affy axiom dataTypical
- rs555879MYO5B · 49,826,163G;Gcommon in clinvarTypical
- rs17715416MYO5B · 49,962,255A;Acommon in clinvarTypical
- rs58408750,866,180A;GNo summary available.Typical
- rs642698ME2 · 50,896,615G;TNo summary available.Typical
- rs3819122SMAD4 · 51,084,461A;Acommon in clinvarTypical
- rs8096445MEX3C · 51,186,670C;CNo summary available.Typical
- rs9951523DCC · 52,340,854C;Ccommon in complete genomicsTypical
- rs1460196DCC · 52,689,042C;Ccommon genotypeTypical
- rs2270954DCC · 53,530,928A;APossible increased susceptibility to schizophreniaWorth knowing
- rs17594526TCF4 · 55,391,007C;Ccommon in complete genomicsTypical
- rs17595731TCF4 · 55,440,221C;C~20-30x higher risk for Fuchs' dystrophy, a corneal disorderWorth knowing
- rs9960767TCF4 · 55,487,771C;C1.4x increased risk for schizophreniaMinor
- rs10401120TCF4 · 55,525,267C;Ccommon in complete genomicsTypical
- rs17512836TCF4 · 55,527,730T;Tcommon in complete genomicsTypical
- rs17597926TCF4 · 55,538,707G;Gcommon in complete genomicsTypical
- rs613872TCF4 · 55,543,071G;G~20-30x higher risk for Fuchs' dystrophy, a corneal disorderWorth knowing
- rs995415355,871,026G;G~5x higher risk for Fuchs' dystrophy, a corneal disorderWorth knowing
- rs2286812RPL12P10 · 56,050,233T;T~4x higher risk for Fuchs' dystrophy, a corneal disorderWorth knowing
- rs2272783FECH · 57,571,588G;Glikely erythropoietic protoporphyria symptomsVery important
- rs1041951FECH · 57,573,273C;Ccommon on affy axiom dataTypical
- rs3848519FECH · 57,580,104A;Alikely to be a benign variantMinor
- rs222581ATP8B1 · 57,650,444T;Tcommon in complete genomicsTypical
- rs12968116ATP8B1 · 57,655,270C;Ccommon on affy axiom dataTypical
- rs10503019ATP8B1 · 57,787,145G;GNo summary available.Typical
- rs4149601NEDD4L · 58,149,559G;Gcommon in clinvarTypical
- rs3865418NEDD4L · 58,336,932C;CnormalTypical
- rs103775759,084,822G;Gcommon in complete genomicsTypical
- rs17782313MC4R · 60,183,864C;Cadults likely to be 0.44 BMI units higherWorth knowing
- rs10871777MC4R · 60,184,530G;Gadults likely to be 0.44 BMI units higherWorth knowing
- rs48969360,215,554C;Ccommon in clinvarTypical
- rs12970134MC4R · 60,217,517A;Aadult waist 1.8cm larger on averageTypical
- rs194322660,367,971T;Tcommon in complete genomicsTypical
- rs2229616MC4R · 60,372,043T;Tlower risk of metabolic syndromeWorth knowing
- rs1187813360,399,804T;Tcommon in complete genomicsTypical
- rs216830360,708,701A;Acommon genotypeTypical
- rs12956925TNFRSF11A · 62,346,407A;ANo summary available.Typical
- rs1805034TNFRSF11A · 62,360,008C;Ccommon in clinvarTypical
- rs8093550LINC01924 · 64,210,542T;TNo summary available.Typical
- rs212434967,349,863G;Gcommon in complete genomicsTypical
- rs17077540LOC643542 · 67,618,042A;G1.6x major depressive disorder riskWorth knowing
- rs13353224LOC105372173 · 67,733,188A;Acommon on affy axiom dataTypical
- rs763361CD226 · 69,864,406T;TIncreased risk for multiple autoimmune diseasesWorth knowing
- rs266091770,960,842T;TNo summary available.Typical
- rs1708384471,175,007G;Gcommon in complete genomicsTypical
- rs17085106LINC01899 · 71,771,837G;Gcommon in complete genomicsTypical
- rs17086172CBLN2 · 72,559,786T;Tcommon genotypeTypical
- rs41418949NETO1 · 72,774,833C;CNo summary available.Typical
- rs194381673,391,387A;Acommon in complete genomicsTypical
- rs17089362CNDP2 · 74,518,403G;GNo summary available.Typical
- rs890336CNDP2 · 74,520,377T;Tcommon in complete genomicsTypical
- rs890335CNDP2 · 74,521,017G;Gcommon in complete genomicsTypical
- rs12717111CNDP2 · 74,522,015A;Acommon in complete genomicsTypical
- rs17056274LOC105372194 · 75,075,090A;Acommon genotypeTypical
- rs994878475,185,206G;Gcommon genotypeTypical
- rs194319975,750,899G;Gcommon genotypeTypical
- rs6565887ZNF516 · 76,471,019T;TNo summary available.Typical
- rs11663697MBP · 77,023,179G;Gcommon genotypeTypical
- rs1166185677,941,567G;Gcommon 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.