rs397507639

Orientation

plus

Stabilized

plus

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

Make rs397507639(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337120

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507639
dbSNP (classic)	rs397507639
ClinGen	rs397507639
ebi	rs397507639
HLI	rs397507639
Exac	rs397507639
Gnomad	rs397507639
Varsome	rs397507639
LitVar	rs397507639
Map	rs397507639
PheGenI	rs397507639
Biobank	rs397507639
1000 genomes	rs397507639
hgdp	rs397507639
ensembl	rs397507639
geneview	rs397507639
scholar	rs397507639
google	rs397507639
pharmgkb	rs397507639
gwascentral	rs397507639
openSNP	rs397507639
23andMe	rs397507639
SNPshot	rs397507639
SNPdbe	rs397507639
MSV3d	rs397507639
GWAS Ctlg	rs397507639

Max Magnitude

6

ClinVar
Risk	rs397507639(T;T)
Alt	rs397507639(T;T)
Reference	Rs397507639(-;-)
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.32911257dupT
CLNSRC	ClinVar
CLNACC	RCV000044050.2, RCV000256557.2,