SNP Directory

450,817 genetic variants in our database.

All (450,817) Health Risk (400,964) Other (47,777) Drug Response (1,898) Trait (128) Protective (50)
RSID Gene Category Clinical Significance Conditions
RS56136737 ERMAP Trait Affects RADIN BLOOD GROUP ANTIGEN, RADIN BLOOD GROUP ANTIGEN
RS56204206 SEMA7A Trait Affects John Milton Hagen blood group system, John Milton Hagen blood group system
RS56340844 ART4 Trait Affects Blood group, Dombrock system
RS56367230 SEMA7A Trait Affects John Milton Hagen blood group system, John Milton Hagen blood group system
RS56392308 ABO Trait Affects ABO blood group system, ABO blood group system
RS566629828 SMIM1 Trait Affects Vel blood group system, Vel blood group system
RS587776861 AFP Trait Affects Alpha-fetoprotein, hereditary persistence of
RS587777831 ART4 Trait Affects Blood group, Dombrock system
RS587777832 ART4 Trait Affects Blood group, Dombrock system
RS587777833 ART4 Trait Affects Blood group, Dombrock system
RS62542743 AQP7 Trait Affects GLYCEROL QUANTITATIVE TRAIT LOCUS, Cervical cancer
RS642742 KITLG Trait Affects SKIN/HAIR/EYE PIGMENTATION 7, DARK/LIGHT SKIN
RS74315453 A4GALT Trait Affects p phenotype, p phenotype
RS74315454 A4GALT Trait Affects p phenotype, p phenotype
RS746408116 PLA2G5 Trait Affects Familial benign flecked retina, Familial benign flecked retina
RS746908478 DNAJC16 Trait Affects Hereditary spastic paraplegia, Hereditary spastic paraplegia
RS748544120 SHPK Trait Affects Isolated sedoheptulokinase deficiency, Isolated sedoheptulokinase deficiency
RS748728975 STAB1 Trait Affects Isolated hyperferritinemia, Isolated hyperferritinemia
RS750303687 CUBN Trait Affects Proteinuria, chronic benign
RS751995528 B3GALNT1 Trait Affects p phenotype, p phenotype
RS754318051 STAB1 Trait Affects Isolated hyperferritinemia, Isolated hyperferritinemia
RS754663945 KEL Trait Affects Kell blood group system, Kell blood group system
RS765925019 ABCB6 Trait Affects Langereis blood group, Langereis blood group
RS766454085 PLA2G5 Trait Affects Familial benign flecked retina, Familial benign flecked retina
RS768027884 SEMA3F Trait Affects Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism
RS77493670 ICAM4 Trait Affects Landsteiner-Wiener phenotype, Landsteiner-Wiener phenotype
RS776678047 GSTZ1 Trait Affects Maleylacetoacetate isomerase deficiency, Maleylacetoacetate isomerase deficiency
RS777011308 KEL Trait Affects Kell blood group system, Kell blood group system
RS777137810 NRG1 Trait Affects Hereditary spastic paraplegia, Hereditary spastic paraplegia
RS777313922 SLC14A1 Trait Affects altered red cell phenotype, altered red cell phenotype
RS778248852 ICAM4 Trait Affects Landsteiner-Wiener phenotype, Landsteiner-Wiener phenotype
RS782544248 ABO Trait Benign; Affects ABO blood group system, Severely weakened expression of A on erythrocytes
RS797044429 KNG1 Trait Affects High molecular weight kininogen deficiency, High molecular weight kininogen deficiency
RS797044430 KNG1 Trait Affects High molecular weight kininogen deficiency, High molecular weight kininogen deficiency
RS869183622 - Trait Affects Venous thromboembolism, Venous thromboembolism
RS869312818 CD55 Trait Affects Cromer blood group system, Cromer blood group system
RS869320718 KNG1 Trait Affects High molecular weight kininogen deficiency, High molecular weight kininogen deficiency
RS879255549 ABCB6 Trait Affects Langereis blood group, Langereis blood group
RS879255550 RHD Trait Affects Blood group antigen abnormality, Blood group antigen abnormality
RS916977 HERC2 Trait Affects SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES
RS10 — Other — —
RS1000113 — Other — —
RS10002492 — Other — —
RS1000283 — Other — —
RS1000294 — Other — —
RS10003447 — Other — —
RS10004195 — Other — —
RS10004839 — Other — —
RS10005233 — Other — —
RS10005603 — Other — —
RS1000579 — Other — —
RS1000589 — Other — —
RS1000592 — Other — —
RS1000597 — Other — —
RS10007052 — Other — —
RS10007186 — Other — —
RS1000731 — Other — —
RS1000735 — Other — —
RS10007590 — Other — —
RS1000778 — Other — —
RS10008257 — Other — —
RS10008492 — Other — —
RS10009145 — Other — —
RS1000916 — Other — —
RS10009228 — Other — —
RS10010131 — Other — —
RS1001021 — Other — —
RS10010325 — Other — —
RS10010758 — Other — —
RS1001139 — Other — —
RS1001179 — Other — —
RS10011926 — Other — —
RS10012 — Other — —
RS10012307 — Other — —
RS10012946 — Other — —
RS10012953 — Other — —
RS10013040 — Other — —
RS10013166 — Other — —
RS10013228 — Other — —
RS10014072 — Other — —
RS1001579 — Other — —
RS10017238 — Other — —
RS10017284 — Other — —
RS1001761 — Other — —
RS10017674 — Other — —
RS10018204 — Other — —
RS10018239 — Other — —
RS10018902 — Other — —
RS10019009 — Other — —
RS10019888 — Other — —
RS10020432 — Other — —
RS10020464 — Other — —
RS1002076 — Other — —
RS10021303 — Other — —
RS10021308 — Other — —
RS1002205 — Other — —
RS10022462 — Other — —
RS10022537 — Other — —
RS10023464 — Other — —
RS10024217 — Other — —
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