Rs104894147

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894147(G;G)
Make rs104894147(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102835350
GeneCYP17A1
is asnp
is mentioned by
dbSNPrs104894147
Exacrs104894147
PheGenIrs104894147
nextbiors104894147
hapmaprs104894147
1000 genomesrs104894147
hgdprs104894147
ensemblrs104894147
gopubmedrs104894147
geneviewrs104894147
scholarrs104894147
googlers104894147
pharmgkbrs104894147
gwascentralrs104894147
openSNPrs104894147
23andMers104894147
23andMe allrs104894147
SNP Nexus

SNPshotrs104894147
SNPdbers104894147
MSV3drs104894147
OMIM609300
Desc
Variant0019
Relatedalso
ClinVar
Risk rs104894147(G;G)
Alt rs104894147(G;G)
Reference rs104894147(T;T)
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.104595107A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001865.2,