Chromosome 14
196 well-documented SNPs on chromosome 14, in order of position (GRCh38).
- rs1049564PNP · 20,472,447G;Gcommon in clinvarTypical
- rs124370420,536,903G;Gcommon genotypeTypical
- rs11701ANG · 20,693,894T;Tcommon in clinvarTypical
- rs10151259RPGRIP1 · 21,321,881T;TRecessive genotype uncertain pathogenicityWorth knowing
- rs17103671RPGRIP1 · 21,343,037A;Acommon in clinvarTypical
- rs12587781TRA@ · 22,530,666G;T1.79x increased risk for narcolepsy in Europeans and 1.34x in AsiansTypical
- rs1154155TRA · 22,533,736G;G2.5x increased risk for narcolepsyWorth knowing
- rs17880989MMP14 · 22,844,424G;Gcommon genotypeTypical
- rs3751489MMP14 · 22,844,771G;Gcommon in complete genomicsTypical
- rs4982731CEBPE · 23,116,124C;CPossible higher risk of childhood acute lymphoblastic leukemiaMinor
- rs2239633CEBPE · 23,119,848G;GNo summary available.Typical
- rs1055061HOMEZ · 23,275,723C;Ccommon in complete genomicsTypical
- rs2231801EFS · 23,360,281C;CNo summary available.Typical
- rs365990MYH6 · 23,392,602G;Grisk genotypeMinor
- rs452036MYH6 · 23,396,676G;Gcommon in clinvarTypical
- rs2754157MYH7 · 23,418,010T;Tcommon in complete genomicsTypical
- rs45496496MYH7 · 23,423,939C;GVariant of unclear significanceImportant
- rs3218716MYH7 · 23,425,316C;TFamilial hypertrophic cardiomyopathy (possible)Very important
- rs121913626MYH7 · 23,427,723C;GFamilial Hypertrophic CardiomyopathyVery important
- rs4981473MYH7 · 23,428,966C;Ccommon in clinvarTypical
- rs3218714MYH7 · 23,429,279C;GFamilial Hypertrophic CardiomyopathyVery important
- rs3218713MYH7 · 23,431,468A;CFamilial Hypertrophic CardiomyopathyVery important
- rs2281680LOC102724814 · 23,563,861C;Ccommon on affy axiom dataTypical
- rs3021119PCK2 · 24,098,289C;Ccommon in complete genomicsTypical
- rs10141896NFATC4 · 24,376,196G;Gcommon in complete genomicsTypical
- rs2877649LOC101927045 · 24,484,796C;Ccommon genotypeTypical
- rs8192917LOC107984667 · 24,632,954T;TNo summary available.Typical
- rs1258677425,660,360G;Gcommon genotypeTypical
- rs1711192026,937,686G;Gcommon in complete genomicsTypical
- rs2877832LOC728755 · 27,330,971C;Ccommon on affy axiom dataTypical
- rs1184769730,045,906C;Ccommon in complete genomicsTypical
- rs1045644COCH · 30,885,890C;Ccommon in clinvarTypical
- rs7157080AP4S1 · 31,084,514T;Tcommon in complete genomicsTypical
- rs8004379NPAS3 · 33,599,495A;Acommon in complete genomicsTypical
- rs1048990PSMA6 · 35,292,469C;C> 1.48x riskTypical
- rs696NFKBIA · 35,401,887C;Ccommon in clinvarTypical
- rs8904NFKBIA · 35,402,011G;Gcommon in clinvarTypical
- rs94428936,180,040T;T1.69x increased thyroid cancer riskWorth knowing
- rs2076751NKX2-1-AS1 · 36,520,214C;Ccommon in clinvarTypical
- rs17104630LOC105370453 · 36,530,844A;Acommon in complete genomicsTypical
- rs17107115TTC6 · 37,795,751G;GNo summary available.Typical
- rs12896790TTC6 · 37,804,717T;Tcommon on affy axiom dataTypical
- rs1049834538,551,301A;A<0.5x decreased risk for coronary spasmTypical
- rs7140561LOC100288846 · 39,267,476C;Ccommon in complete genomicsTypical
- rs1053667FAM179B · 45,073,835T;Tcommon genotypeTypical
- rs17118552MDGA2 · 47,405,354A;Acommon in complete genomicsTypical
- rs8004608MDGA2 · 47,618,211T;Tcommon in complete genomicsTypical
- rs2225994LOC105378178 · 48,605,716T;Tcommon genotypeTypical
- rs11845208LOC105378178 · 48,994,281A;Acommon genotypeTypical
- rs2073347NIN · 50,757,071C;Ccommon in clinvarTypical
- rs2236316NIN · 50,757,699G;Gcommon in clinvarTypical
- rs946616PYGL · 50,921,064C;Ccommon in complete genomicsTypical
- rs7142143PYGL · 50,936,813C;CIncreased odds of relapse in treated childhood ALL patientsWorth knowing
- rs1380131LOC105370504 · 53,606,140C;Ccommon on affy axiom dataTypical
- rs12431733LOC105370503 · 53,824,112T;TIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs17563BMP4 · 53,950,804G;GRisk for otosclerosisWorth knowing
- rs17127713SAMD4A · 54,656,200A;Acommon genotypeTypical
- rs17738966GCH1 · 54,835,501G;GNo summary available.Typical
- rs10483639GCH1 · 54,839,739G;Gcommon/normalTypical
- rs841GCH1 · 54,843,774A;Adecreased baroreflex sensitivity, heart rate variability, and in women, hypertensionWorth knowing
- rs41298442GCH1 · 54,844,099C;CDystonia (dopa-responsive) from homozygous GCH1 mutationVery important
- rs752688GCH1 · 54,844,851C;Ccommon/normalTypical
- rs4411417GCH1 · 54,853,845T;Tcommon/normalTypical
- rs998259GCH1 · 54,888,313C;Ccommon/normalTypical
- rs3783641GCH1 · 54,893,421T;Tcommon/normalTypical
- rs8007267GCH1 · 54,912,273C;Ccommon/normalTypical
- rs1676MAPK1IP1L · 55,067,973G;Gcommon in complete genomicsTypical
- rs1495465LOC105370519 · 57,549,696C;Ccommon in complete genomicsTypical
- rs10134944SLC35F4 · 57,652,478C;T1.4x risk of bipolar disorder.Minor
- rs8013190SLC35F4 · 57,888,330A;Acommon in complete genomicsTypical
- rs10130695PPM1A · 60,289,266C;CNo summary available.Typical
- rs767603LOC105378189 · 60,631,965C;C0.63x reduced risk for intracranial aneurysmTypical
- rs6573333MNAT1 · 60,841,619G;Gcommon genotypeTypical
- rs3783799PRKCH · 61,452,498T;T1.4x increased risk for strokeTypical
- rs2230500PRKCH · 61,457,521A;A1.4x increased risk for strokeTypical
- rs11549465HIF1A · 61,740,839C;Ccommon on affy axiom dataTypical
- rs11549467HIF1A · 61,740,857G;Gcommon in complete genomicsTypical
- rs4902100SYT16 · 62,083,101A;Acommon/normalTypical
- rs97396862,187,980A;ANo summary available.Typical
- rs4902141LOC105370529 · 62,501,677T;TNo summary available.Typical
- rs1152591SYNE2 · 64,214,130G;Gcommon/normalTypical
- rs1255998ESR2 · 64,227,153G;Gcommon in complete genomicsTypical
- rs8018687ESR2 · 64,227,364T;Tcommon in complete genomicsTypical
- rs1256062ESR2 · 64,236,600T;Tcommon in complete genomicsTypical
- rs1256049ESR2 · 64,257,333C;Ccommon in complete genomicsTypical
- rs1271572ESR2 · 64,295,199C;CnormalTypical
- rs10483774ESR2 · 64,296,881G;Gcommon in complete genomicsTypical
- rs2987983ESR2 · 64,296,935G;G1.2x increased risk of prostate cancerWorth knowing
- rs8003379MTHFD1 · 64,406,881A;AnormalTypical
- rs1950902MTHFD1 · 64,415,662A;Acommon in clinvarTypical
- rs10498514MTHFD1 · 64,432,337A;Acommon in complete genomicsTypical
- rs2295639MTHFD1 · 64,435,398T;Tcommon in complete genomicsTypical
- rs2236225MTHFD1 · 64,442,127A;ASlightly (~1.5x) higher risk for Caucasian mothers to give birth to NTD childrenMinor
- rs2269310SPTB · 64,770,485G;Gcommon in complete genomicsTypical
- rs1957949MAX · 65,075,889C;Ccommon in clinvarTypical
- rs1957948MAX · 65,075,911C;Ccommon in clinvarTypical
- rs4902359MAX · 65,076,072G;Gcommon in clinvarTypical
- rs1256531PTBP1P · 65,281,041A;ANo summary available.Typical
- rs12894182FUT8 · 65,471,171C;Ccommon in complete genomicsTypical
- rs35949016FUT8 · 65,669,445C;Ccommon on affy axiom dataTypical
- rs12891047ZFYVE26 · 67,776,358A;Acommon/normalTypical
- rs8017304RAD51B · 68,318,360G;Gcommon in clinvarTypical
- rs999737RAD51L1 · 68,567,965C;Ccommon on affy axiom dataTypical
- rs1717522770,035,333G;Gcommon genotypeTypical
- rs10143078SYNJ2BP · 70,414,772A;Acommon genotypeTypical
- rs17108533MAP3K9 · 70,783,085C;Ccommon on affy axiom dataTypical
- rs699363RGS6 · 72,225,785A;Acommon in complete genomicsTypical
- rs2074647RGS6 · 72,562,470G;Gcommon on affy axiom dataTypical
- rs12587742DCAF4 · 72,926,683A;ASlightly increased (1.18x) risk for lung cancerMinor
- rs1800844PSEN1 · 73,136,992G;Gcommon in complete genomicsTypical
- rs63749824PSEN1 · 73,170,945C;Tassociated with Alzheimer's disease (either early- or late-onset)Very important
- rs63750306PSEN1 · 73,173,663A;CAlzheimer's diseaseVery important
- rs63750391PSEN1 · 73,173,665A;GAlzheimer's disease (reported; but see discussion)Very important
- rs63749911PSEN1 · 73,186,901C;TAlzheimer's diseaseVery important
- rs63749891PSEN1 · 73,198,094C;Gearly-onset Alzheimers diseaseVery important
- rs63750231PSEN1 · 73,198,100A;CEarly-onset Alzheimer's disease (in some cases)Very important
- rs17125721PSEN1 · 73,206,470A;Acommon in clinvarTypical
- rs63750083PSEN1 · 73,219,177A;CEarly-onset Alzheimer's; see discussionVery important
- rs362344PSEN1 · 73,223,011C;Ccommon in clinvarTypical
- rs108621MLH3 · 75,013,934T;Tcommon in clinvarTypical
- rs175080MLH3 · 75,047,125G;Gcommon in clinvarTypical
- rs175081MLH3 · 75,047,180C;Ccommon in complete genomicsTypical
- rs28756991MLH3 · 75,047,266C;Ccommon in complete genomicsTypical
- rs28756990MLH3 · 75,047,435C;Ccommon in clinvarTypical
- rs910316TMED10 · 75,159,339C;C0.68cm taller on averageTypical
- rs724743TTLL5 · 75,663,248A;Acommon in complete genomicsTypical
- rs93533476,147,335C;Ccommon in complete genomicsTypical
- rs2121070C14orf118 · 76,184,421C;Ccommon in complete genomicsTypical
- rs7972GSTZ1 · 77,326,894G;Gcommon in complete genomicsTypical
- rs177216NRXN3 · 78,063,343G;Gcommon in complete genomicsTypical
- rs221497NRXN3 · 79,622,137G;Gcommon in complete genomicsTypical
- rs225014DIO2 · 80,203,237C;C1.3-1.79x risk of osteoarthritis, 3.75x bipolar, etc.Important
- rs12885300DIO2 · 80,211,923C;CCombined with rs225014, risk of osteoarthritis and bipolar disorderImportant
- rs12587252CEP128 · 80,939,578C;Ccommon genotypeTypical
- rs179247TSHR · 80,966,202A;A>1.3 risk for Graves' diseaseMinor
- rs12101255TSHR · 80,984,708C;T>1.4 risk for Graves' diseaseMinor
- rs2075173LOC101928462 · 81,088,273A;Acommon in complete genomicsTypical
- rs8017455LOC101928462 · 81,109,110T;Tcommon in complete genomicsTypical
- rs3783938LOC101928462 · 81,128,036C;Ccommon in complete genomicsTypical
- rs1991517LOC101928462 · 81,144,239C;Cno association with increased bone density and TSHMinor
- rs7144481TSHR · 81,144,598C;Ccommon in clinvarTypical
- rs2288493TSHR · 81,145,262C;Ccommon in clinvarTypical
- rs195912281,871,321T;Tcommon genotypeTypical
- rs22981383,452,020C;Ccommon in complete genomicsTypical
- rs1162405687,039,904A;Acommon in complete genomicsTypical
- rs421262GALC · 87,934,869C;Ccommon in complete genomicsTypical
- rs8005161GPR65 · 88,006,251C;Ccommon in complete genomicsTypical
- rs1712458188,360,338T;Tcommon on affy axiom dataTypical
- rs28365054TDP1 · 89,963,514G;Gcommon in clinvarTypical
- rs5871CALM1 · 90,405,134T;Tcommon in complete genomicsTypical
- rs2273647PPP4R3A · 91,461,942C;TSome protective effect against Alzheimer's by preventing brain glucose declineWorth knowing
- rs12896399LOC105370627 · 92,307,319T;TLighter hair color & blue eyes more likelyTypical
- rs8019291SLC24A4 · 92,464,820G;Gcommon in complete genomicsTypical
- rs10498635RIN3 · 92,636,964C;Ccommon on affy axiom dataTypical
- rs131650692,918,108G;Gcommon in complete genomicsTypical
- rs941601SERPINA6 · 94,305,204C;Ccommon in complete genomicsTypical
- rs1243168SERPINA1 · 94,375,029A;ASomewhat increased risk for chronic rhinosinusitis?Worth knowing
- rs11832SERPINA1 · 94,377,228T;Tcommon in clinvarTypical
- rs1243166SERPINA1 · 94,377,481G;Gcommon/normalTypical
- rs1243164SERPINA1 · 94,378,133C;Ccommon in clinvarTypical
- rs1303SERPINA1 · 94,378,506T;Tcommon in clinvarTypical
- rs121912713SERPINA1 · 94,378,561A;CBleeding disorder likelyVery important
- rs28929474SERPINA1 · 94,378,610T;TAlpha-1 Antitrypsin DeficiencyVery important
- rs11846959SERPINA1 · 94,379,979G;Gcommon/normalTypical
- rs17580SERPINA1 · 94,380,925A;Aa slightly reduced functionality form of Alpha-1 Antitrypsin DeficiencyWorth knowing
- rs6647SERPINA1 · 94,381,078G;GNormal; two copies of Pi-M1A alleleTypical
- rs20546SERPINA1 · 94,382,814G;Gcommon in clinvarTypical
- rs709932SERPINA1 · 94,382,864G;GNo summary available.Typical
- rs2749531SERPINA1 · 94,386,355G;Gcommon in complete genomicsTypical
- rs1243160SERPINA1 · 94,388,540G;Gcommon/normalTypical
- rs7151526SERPINA1 · 94,397,299A;Apossible increased risk for ANCA associated vasculitisMinor
- rs4934SERPINA3 · 94,614,466A;A2.5x increased risk of Azheimer's and decreased age at onsetTypical
- rs17473SERPINA3 · 94,619,305C;Ccommon in clinvarTypical
- rs3742330DICER1 · 95,087,025A;Acommon in clinvarTypical
- rs1057035DICER1 · 95,087,805T;Tcommon in clinvarTypical
- rs13078DICER1 · 95,090,410A;Acommon in clinvarTypical
- rs1243226095,381,957C;Ccommon genotypeTypical
- rs7158782TCL1A · 95,702,794G;G4x higher risk of adverse side-effect if taking aromatase inhibitorVery important
- rs945032BDKRB2 · 96,204,324C;CNo summary available.Typical
- rs1799722BDKRB2 · 96,204,802T;TAssociated with endurance performanceMinor
- rs801662096,927,348T;Tcommon genotypeTypical
- rs1048412898,176,235C;Ccommon in complete genomicsTypical
- rs145914898,374,106C;Ccommon in complete genomicsTypical
- rs1162371398,773,979A;GNo summary available.Typical
- rs750610248BCL11B · 99,175,513A;Acommon in clinvarTypical
- rs1802710DLK1 · 100,734,308C;Tcommon in complete genomicsTypical
- rs10145110101,008,533C;Ccommon genotypeTypical
- rs11844707MIR381HG · 101,044,276G;Gcommon in complete genomicsTypical
- rs7142002PPP2R5C · 101,894,408T;Tcommon in complete genomicsTypical
- rs10133111TRAF3 · 102,910,984G;Gcommon in complete genomicsTypical
- rs1052912TNFAIP2 · 103,137,316G;GNo summary available.Typical
- rs17679127MARK3 · 103,423,754A;Acommon in complete genomicsTypical
- rs8702KLC1 · 103,686,015G;GaverageTypical
- rs3212057XRCC3 · 103,707,128C;Ccommon in complete genomicsTypical
- rs11622475TDRD9 · 104,042,739C;C1.5x risk of bipolar disorderTypical
- rs2494732AKT1 · 104,772,855C;Cgreater odds of cannabis-associated psychosisWorth knowing
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.