rs397508909

Orientation

minus

Stabilized

minus

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

Make rs397508909(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093723

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508909
dbSNP (classic)	rs397508909
ClinGen	rs397508909
ebi	rs397508909
HLI	rs397508909
Exac	rs397508909
Gnomad	rs397508909
Varsome	rs397508909
LitVar	rs397508909
Map	rs397508909
PheGenI	rs397508909
Biobank	rs397508909
1000 genomes	rs397508909
hgdp	rs397508909
ensembl	rs397508909
geneview	rs397508909
scholar	rs397508909
google	rs397508909
pharmgkb	rs397508909
gwascentral	rs397508909
openSNP	rs397508909
23andMe	rs397508909
SNPshot	rs397508909
SNPdbe	rs397508909
MSV3d	rs397508909
GWAS Ctlg	rs397508909

Max Magnitude

6

ClinVar
Risk	rs397508909(G;G)
Alt	rs397508909(G;G)
Reference	Rs397508909(C;C)
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.41245740G>C
CLNSRC	ClinVar
CLNACC	RCV000047592.2, RCV000256524.2,