rs397507711

Orientation

plus

Stabilized

plus

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

Make rs397507711(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338526

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507711
dbSNP (classic)	rs397507711
ClinGen	rs397507711
ebi	rs397507711
HLI	rs397507711
Exac	rs397507711
Gnomad	rs397507711
Varsome	rs397507711
LitVar	rs397507711
Map	rs397507711
PheGenI	rs397507711
Biobank	rs397507711
1000 genomes	rs397507711
hgdp	rs397507711
ensembl	rs397507711
geneview	rs397507711
scholar	rs397507711
google	rs397507711
pharmgkb	rs397507711
gwascentral	rs397507711
openSNP	rs397507711
23andMe	rs397507711
SNPshot	rs397507711
SNPdbe	rs397507711
MSV3d	rs397507711
GWAS Ctlg	rs397507711

Max Magnitude

6

ClinVar
Risk	rs397507711(-;-)
Alt	rs397507711(-;-)
Reference	Rs397507711(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.32912663delG
CLNSRC	ClinVar
CLNACC	RCV000044366.2, RCV000241238.2,