rs397508003

Orientation

plus

Stabilized

plus

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

Make rs397508003(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32376754

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508003
dbSNP (classic)	rs397508003
ClinGen	rs397508003
ebi	rs397508003
HLI	rs397508003
Exac	rs397508003
Gnomad	rs397508003
Varsome	rs397508003
LitVar	rs397508003
Map	rs397508003
PheGenI	rs397508003
Biobank	rs397508003
1000 genomes	rs397508003
hgdp	rs397508003
ensembl	rs397508003
geneview	rs397508003
scholar	rs397508003
google	rs397508003
pharmgkb	rs397508003
gwascentral	rs397508003
openSNP	rs397508003
23andMe	rs397508003
SNPshot	rs397508003
SNPdbe	rs397508003
MSV3d	rs397508003
GWAS Ctlg	rs397508003

Max Magnitude

6

ClinVar
Risk	rs397508003(-;-)
Alt	rs397508003(-;-)
Reference	Rs397508003(AA;AA)
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.32950891_32950892delAA
CLNSRC	ClinVar
CLNACC	RCV000045607.2, RCV000257064.2,