rs397507691

Orientation

plus

Stabilized

plus

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

Make rs397507691(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338202

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507691
dbSNP (classic)	rs397507691
ClinGen	rs397507691
ebi	rs397507691
HLI	rs397507691
Exac	rs397507691
Gnomad	rs397507691
Varsome	rs397507691
LitVar	rs397507691
Map	rs397507691
PheGenI	rs397507691
Biobank	rs397507691
1000 genomes	rs397507691
hgdp	rs397507691
ensembl	rs397507691
geneview	rs397507691
scholar	rs397507691
google	rs397507691
pharmgkb	rs397507691
gwascentral	rs397507691
openSNP	rs397507691
23andMe	rs397507691
SNPshot	rs397507691
SNPdbe	rs397507691
MSV3d	rs397507691
GWAS Ctlg	rs397507691

Max Magnitude

6

ClinVar
Risk	rs397507691(-;-)
Alt	rs397507691(-;-)
Reference	Rs397507691(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.32912339delG
CLNSRC	ClinVar
CLNACC	RCV000044281.2, RCV000257712.2,