rs104894136

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs104894136(C;T)

Make rs104894136(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

102834074

Gene	CYP17A1, CYP17A1-AS1

is a	snp
is	mentioned by
dbSNP	rs104894136
dbSNP (classic)	rs104894136
ClinGen	rs104894136
ebi	rs104894136
HLI	rs104894136
Exac	rs104894136
Gnomad	rs104894136
Varsome	rs104894136
LitVar	rs104894136
Map	rs104894136
PheGenI	rs104894136
Biobank	rs104894136
1000 genomes	rs104894136
hgdp	rs104894136
ensembl	rs104894136
geneview	rs104894136
scholar	rs104894136
google	rs104894136
pharmgkb	rs104894136
gwascentral	rs104894136
openSNP	rs104894136
23andMe	rs104894136
SNPshot	rs104894136
SNPdbe	rs104894136
MSV3d	rs104894136
GWAS Ctlg	rs104894136

Max Magnitude

0

c.715C>T (p.Arg239Ter)

23andMe name: i5001494

OMIM	609300
Desc
Variant	0006
Related	also

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,