rs397508891

Orientation

minus

Stabilized

minus

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

Make rs397508891(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093907

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508891
dbSNP (classic)	rs397508891
ClinGen	rs397508891
ebi	rs397508891
HLI	rs397508891
Exac	rs397508891
Gnomad	rs397508891
Varsome	rs397508891
LitVar	rs397508891
Map	rs397508891
PheGenI	rs397508891
Biobank	rs397508891
1000 genomes	rs397508891
hgdp	rs397508891
ensembl	rs397508891
geneview	rs397508891
scholar	rs397508891
google	rs397508891
pharmgkb	rs397508891
gwascentral	rs397508891
openSNP	rs397508891
23andMe	rs397508891
SNPshot	rs397508891
SNPdbe	rs397508891
MSV3d	rs397508891
GWAS Ctlg	rs397508891

Max Magnitude

6

aka c.787+836dup

ClinVar
Risk	rs397508891(G;G)
Alt	rs397508891(G;G)
Reference	Rs397508891(-;-)
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.41245925dupC
CLNSRC	ClinVar
CLNACC	RCV000047544.2, RCV000257065.2,