rs397508903

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6	BRCA1 variant considered pathogenic for breast cancer

Make rs397508903(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093802

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508903
dbSNP (classic)	rs397508903
ClinGen	rs397508903
ebi	rs397508903
HLI	rs397508903
Exac	rs397508903
Gnomad	rs397508903
Varsome	rs397508903
LitVar	rs397508903
Map	rs397508903
PheGenI	rs397508903
Biobank	rs397508903
1000 genomes	rs397508903
hgdp	rs397508903
ensembl	rs397508903
geneview	rs397508903
scholar	rs397508903
google	rs397508903
pharmgkb	rs397508903
gwascentral	rs397508903
openSNP	rs397508903
23andMe	rs397508903
SNPshot	rs397508903
SNPdbe	rs397508903
MSV3d	rs397508903
GWAS Ctlg	rs397508903

Max Magnitude

6

ClinVar
Risk	rs397508903(C;C) rs397508903(T;T)
Alt	rs397508903(C;C) rs397508903(T;T)
Reference	Rs397508903(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41245819C>A
CLNSRC	ClinVar
CLNACC	RCV000047570.2, RCV000257813.2,