Rs104894148

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894148(A;T)
Make rs104894148(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102835343
GeneCYP17A1
is asnp
is mentioned by
dbSNPrs104894148
Exacrs104894148
PheGenIrs104894148
nextbiors104894148
hapmaprs104894148
1000 genomesrs104894148
hgdprs104894148
ensemblrs104894148
gopubmedrs104894148
geneviewrs104894148
scholarrs104894148
googlers104894148
pharmgkbrs104894148
gwascentralrs104894148
openSNPrs104894148
23andMers104894148
23andMe allrs104894148
SNP Nexus

SNPshotrs104894148
SNPdbers104894148
MSV3drs104894148
Max Magnitude0
OMIM609300
Desc
Variant0020
Relatedalso
ClinVar
Risk rs104894148(T;T)
Alt rs104894148(T;T)
Reference rs104894148(A;A)
Significance Pathogenic
Disease Combined partial 17-alpha-hydroxylase/17
Variation info
Gene CYP17A1
CLNDBN Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency
Reversed 1
HGVS NC_000010.10:g.104595100T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001866.2,