Rs104894142

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894142
PheGenIrs104894142
hapmaprs104894142
1000 genomesrs104894142
hgdprs104894142
ensemblrs104894142
gopubmedrs104894142
geneviewrs104894142
scholarrs104894142
googlers104894142
pharmgkbrs104894142
gwascentralrs104894142
openSNPrs104894142
23andMers104894142
23andMe allrs104894142
SNP Nexus

SNPshotrs104894142
SNPdbers104894142
MSV3drs104894142
GeneCYP17A1, CYP17A1-AS1
Chromosome10
Orientationminus
Position102832566
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894142(C;T)
Make rs104894142(T;T)
OMIM609300
Desc
Variant0023
Relatedalso
ClinVar
Risk rs104894142(T;T)
Alt rs104894142(T;T)
Reference rs104894142(C;C)
Significance 5
Disease Complete combined 17-alpha-hydroxylase/17
ClinVar info
Gene CYP17A1
CLNDBN Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency
Reversed 1
CLNHGVS NC_000010.10:g.104592323G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001869.1