rs397507591

Orientation

plus

Stabilized

plus

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

Make rs397507591(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332977

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507591
dbSNP (classic)	rs397507591
ClinGen	rs397507591
ebi	rs397507591
HLI	rs397507591
Exac	rs397507591
Gnomad	rs397507591
Varsome	rs397507591
LitVar	rs397507591
Map	rs397507591
PheGenI	rs397507591
Biobank	rs397507591
1000 genomes	rs397507591
hgdp	rs397507591
ensembl	rs397507591
geneview	rs397507591
scholar	rs397507591
google	rs397507591
pharmgkb	rs397507591
gwascentral	rs397507591
openSNP	rs397507591
23andMe	rs397507591
SNPshot	rs397507591
SNPdbe	rs397507591
MSV3d	rs397507591
GWAS Ctlg	rs397507591

Max Magnitude

6

ClinVar
Risk	rs397507591(-;-)
Alt	rs397507591(-;-)
Reference	Rs397507591(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.32907114delG
CLNSRC	ClinVar
CLNACC	RCV000043818.2, RCV000077258.4,