Rs104894142

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894142(C;T)
Make rs104894142(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102832566
GeneCYP17A1, CYP17A1-AS1
is asnp
is mentioned by
dbSNPrs104894142
Exacrs104894142
PheGenIrs104894142
nextbiors104894142
hapmaprs104894142
1000 genomesrs104894142
hgdprs104894142
ensemblrs104894142
gopubmedrs104894142
geneviewrs104894142
scholarrs104894142
googlers104894142
pharmgkbrs104894142
gwascentralrs104894142
openSNPrs104894142
23andMers104894142
23andMe allrs104894142
SNP Nexus

SNPshotrs104894142
SNPdbers104894142
MSV3drs104894142
OMIM609300
Desc
Variant0023
Relatedalso
ClinVar
Risk rs104894142(T;T)
Alt rs104894142(T;T)
Reference rs104894142(C;C)
Significance Pathogenic
Disease Complete combined 17-alpha-hydroxylase/17
Variation info
Gene CYP17A1
CLNDBN Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency
Reversed 1
HGVS NC_000010.10:g.104592323G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001869.1,