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rs104894136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs104894136(C;T)
Make rs104894136(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102834074
GeneCYP17A1, CYP17A1-AS1
is asnp
is mentioned by
dbSNPrs104894136
dbSNP (classic)rs104894136
ClinGenrs104894136
ebirs104894136
HLIrs104894136
Exacrs104894136
Gnomadrs104894136
Varsomers104894136
LitVarrs104894136
Maprs104894136
PheGenIrs104894136
Biobankrs104894136
1000 genomesrs104894136
hgdprs104894136
ensemblrs104894136
geneviewrs104894136
scholarrs104894136
googlers104894136
pharmgkbrs104894136
gwascentralrs104894136
openSNPrs104894136
23andMers104894136
SNPshotrs104894136
SNPdbers104894136
MSV3drs104894136
GWAS Ctlgrs104894136
Max Magnitude0

c.715C>T (p.Arg239Ter)

23andMe name: i5001494

OMIM609300
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894136(T;T)
Alt rs104894136(T;T)
Reference Rs104894136(C;C)
Significance Other
Disease Combined partial 17-alpha-hydroxylase/17 Breast cancer
Variation info
Gene CYP17A1
CLNDBN Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency Breast cancer, susceptibility to
Reversed 1
HGVS NC_000010.10:g.104593831G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001854.2, RCV000001855.2,