rs397508065

Orientation

plus

Stabilized

plus

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

Make rs397508065(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319106

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508065
dbSNP (classic)	rs397508065
ClinGen	rs397508065
ebi	rs397508065
HLI	rs397508065
Exac	rs397508065
Gnomad	rs397508065
Varsome	rs397508065
LitVar	rs397508065
Map	rs397508065
PheGenI	rs397508065
Biobank	rs397508065
1000 genomes	rs397508065
hgdp	rs397508065
ensembl	rs397508065
geneview	rs397508065
scholar	rs397508065
google	rs397508065
pharmgkb	rs397508065
gwascentral	rs397508065
openSNP	rs397508065
23andMe	rs397508065
SNPshot	rs397508065
SNPdbe	rs397508065
MSV3d	rs397508065
GWAS Ctlg	rs397508065

Max Magnitude

6

ClinVar
Risk	rs397508065(T;T)
Alt	rs397508065(T;T)
Reference	Rs397508065(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.32893243G>T
CLNSRC	ClinVar
CLNACC	RCV000045898.2, RCV000256555.2,