rs397508924

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common/normal
(-;G)	6	BRCA1 variant considered pathogenic for breast cancer
(A;A)	0	common in clinvar

Make rs397508924(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093567

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508924
dbSNP (classic)	rs397508924
ClinGen	rs397508924
ebi	rs397508924
HLI	rs397508924
Exac	rs397508924
Gnomad	rs397508924
Varsome	rs397508924
LitVar	rs397508924
Map	rs397508924
PheGenI	rs397508924
Biobank	rs397508924
1000 genomes	rs397508924
hgdp	rs397508924
ensembl	rs397508924
geneview	rs397508924
scholar	rs397508924
google	rs397508924
pharmgkb	rs397508924
gwascentral	rs397508924
openSNP	rs397508924
23andMe	rs397508924
SNPshot	rs397508924
SNPdbe	rs397508924
MSV3d	rs397508924
GWAS Ctlg	rs397508924

Max Magnitude

6

ClinVar
Risk	rs397508924(G;G) rs397508924(T;T)
Alt	rs397508924(G;G) rs397508924(T;T)
Reference	Rs397508924(-;-)
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.41245584_41245585insC; NC_000017.10:g.41245585dupA
CLNSRC	ClinVar
CLNACC	RCV000047663.2, RCV000257131.1, RCV000047664.2,