Rs104894139

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894139(A;A)
Make rs104894139(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position102832577
GeneCYP17A1, CYP17A1-AS1
is asnp
is mentioned by
dbSNPrs104894139
Exacrs104894139
PheGenIrs104894139
nextbiors104894139
hapmaprs104894139
1000 genomesrs104894139
hgdprs104894139
ensemblrs104894139
gopubmedrs104894139
geneviewrs104894139
scholarrs104894139
googlers104894139
pharmgkbrs104894139
gwascentralrs104894139
openSNPrs104894139
23andMers104894139
23andMe allrs104894139
SNP Nexus

SNPshotrs104894139
SNPdbers104894139
MSV3drs104894139
Max Magnitude0
OMIM609300
Desc
Variant0013
Relatedalso
ClinVar
Risk rs104894139(A;A)
Alt rs104894139(A;A)
Reference rs104894139(G;G)
Significance Pathogenic
Disease Isolated 17
Variation info
Gene CYP17A1
CLNDBN Isolated 17,20-lyase deficiency
Reversed 1
HGVS NC_000010.10:g.104592334C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001861.1,