Rs104894138

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894138(C;T)
Make rs104894138(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102837076
GeneCYP17A1
is asnp
is mentioned by
dbSNPrs104894138
Exacrs104894138
PheGenIrs104894138
nextbiors104894138
hapmaprs104894138
1000 genomesrs104894138
hgdprs104894138
ensemblrs104894138
gopubmedrs104894138
geneviewrs104894138
scholarrs104894138
googlers104894138
pharmgkbrs104894138
gwascentralrs104894138
openSNPrs104894138
23andMers104894138
23andMe allrs104894138
SNP Nexus

SNPshotrs104894138
SNPdbers104894138
MSV3drs104894138
OMIM609300
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104894138(T;T)
Alt rs104894138(T;T)
Reference rs104894138(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.104596833G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001858.2,