rs397508040

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;G)	6	BRCA2 variant considered pathogenic for breast cancer
(G;G)	0	common in clinvar

Make rs397508040(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32380116

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508040
dbSNP (classic)	rs397508040
ClinGen	rs397508040
ebi	rs397508040
HLI	rs397508040
Exac	rs397508040
Gnomad	rs397508040
Varsome	rs397508040
LitVar	rs397508040
Map	rs397508040
PheGenI	rs397508040
Biobank	rs397508040
1000 genomes	rs397508040
hgdp	rs397508040
ensembl	rs397508040
geneview	rs397508040
scholar	rs397508040
google	rs397508040
pharmgkb	rs397508040
gwascentral	rs397508040
openSNP	rs397508040
23andMe	rs397508040
SNPshot	rs397508040
SNPdbe	rs397508040
MSV3d	rs397508040
GWAS Ctlg	rs397508040

Max Magnitude

6

ClinVar
Risk	rs397508040(-;-)
Alt	rs397508040(-;-)
Reference	Rs397508040(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32954253delG
CLNSRC	ClinVar
CLNACC	RCV000045752.2, RCV000241248.2,