ClinVar Miner

List of variants in gene AKR1D1 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP
AKR1D1, 1-BP DEL, 511T
NM_005989.4(AKR1D1):c.*1082G>C rs58526603
NM_005989.4(AKR1D1):c.*1083T>C rs12532715
NM_005989.4(AKR1D1):c.*1085C>T rs12540339
NM_005989.4(AKR1D1):c.*1091C>T rs886062009
NM_005989.4(AKR1D1):c.*1093C>G rs12540340
NM_005989.4(AKR1D1):c.*1095T>C rs61290940
NM_005989.4(AKR1D1):c.*1139G>C rs566511122
NM_005989.4(AKR1D1):c.*1149A>C rs533559202
NM_005989.4(AKR1D1):c.*1151A>G rs548914228
NM_005989.4(AKR1D1):c.*1153C>G rs112833888
NM_005989.4(AKR1D1):c.*1153C>T rs112833888
NM_005989.4(AKR1D1):c.*1163T>C rs11763063
NM_005989.4(AKR1D1):c.*1173A>T rs111628978
NM_005989.4(AKR1D1):c.*1185G>A rs551510105
NM_005989.4(AKR1D1):c.*1199T>A rs886062010
NM_005989.4(AKR1D1):c.*1214A>G rs758246977
NM_005989.4(AKR1D1):c.*1219C>T rs565111801
NM_005989.4(AKR1D1):c.*1265A>G rs113105583
NM_005989.4(AKR1D1):c.*1270T>C rs184548096
NM_005989.4(AKR1D1):c.*1274A>G rs11766258
NM_005989.4(AKR1D1):c.*1282G>A rs534922267
NM_005989.4(AKR1D1):c.*1288A>C rs554615032
NM_005989.4(AKR1D1):c.*1298A>G rs886062011
NM_005989.4(AKR1D1):c.*1311A>C rs188138947
NM_005989.4(AKR1D1):c.*1343C>T rs150650955
NM_005989.4(AKR1D1):c.*1363A>G rs2465921
NM_005989.4(AKR1D1):c.*1372dup rs199524592
NM_005989.4(AKR1D1):c.*1417C>T rs17169522
NM_005989.4(AKR1D1):c.*1484T>C rs17169523
NM_005989.4(AKR1D1):c.*197G>T rs746014627
NM_005989.4(AKR1D1):c.*294C>A rs886062005
NM_005989.4(AKR1D1):c.*298A>G rs886062006
NM_005989.4(AKR1D1):c.*362A>C rs3735023
NM_005989.4(AKR1D1):c.*36C>T rs1872930
NM_005989.4(AKR1D1):c.*373G>A rs564875098
NM_005989.4(AKR1D1):c.*417A>G rs151234162
NM_005989.4(AKR1D1):c.*48C>T rs201088819
NM_005989.4(AKR1D1):c.*507G>A rs7780066
NM_005989.4(AKR1D1):c.*58G>C rs80147006
NM_005989.4(AKR1D1):c.*5A>C rs1872929
NM_005989.4(AKR1D1):c.*879T>C rs73729460
NM_005989.4(AKR1D1):c.*897T>C rs886062007
NM_005989.4(AKR1D1):c.*914C>T rs541055311
NM_005989.4(AKR1D1):c.*944T>C rs886062008
NM_005989.4(AKR1D1):c.21T>G (p.Ser7Arg) rs769312349
NM_005989.4(AKR1D1):c.261+1G>T rs201988060
NM_005989.4(AKR1D1):c.262-7C>A rs144365681
NM_005989.4(AKR1D1):c.316C>T (p.Leu106Phe) rs121918343
NM_005989.4(AKR1D1):c.346C>G (p.Leu116Val) rs886062004
NM_005989.4(AKR1D1):c.380C>T (p.Pro127Leu) rs140421486
NM_005989.4(AKR1D1):c.398C>G (p.Pro133Arg) rs267606649
NM_005989.4(AKR1D1):c.446C>T (p.Ala149Val) rs202238711
NM_005989.4(AKR1D1):c.583G>T (p.Glu195Ter) rs1433614577
NM_005989.4(AKR1D1):c.593C>T (p.Pro198Leu) rs121918342
NM_005989.4(AKR1D1):c.689+1G>T rs575025641
NM_005989.4(AKR1D1):c.781C>T (p.Arg261Cys) rs267606650
NM_005989.4(AKR1D1):c.856-10G>A rs17169518

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