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Rs104894136

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894136
PheGenIrs104894136
nextbiors104894136
hapmaprs104894136
1000 genomesrs104894136
hgdprs104894136
ensemblrs104894136
gopubmedrs104894136
geneviewrs104894136
scholarrs104894136
googlers104894136
pharmgkbrs104894136
gwascentralrs104894136
openSNPrs104894136
23andMers104894136
23andMe allrs104894136
SNP Nexus

SNPshotrs104894136
SNPdbers104894136
MSV3drs104894136
GeneCYP17A1, CYP17A1-AS1
Chromosome10
Orientationminus
Position102834074
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs104894136(C;T)
Make rs104894136(T;T)
OMIM609300
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894136(T;T)
Alt rs104894136(T;T)
Reference rs104894136(C;C)
Significance 255
Disease Combined partial 17-alpha-hydroxylase/17, Breast cancer
ClinVar info
Gene CYP17A1
CLNDBN Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency, Breast cancer, susceptibility to
Reversed 1
CLNHGVS NC_000010.10:g.104593831G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001854.1, RCV000001855.1