rs397507939

Orientation

plus

Stabilized

plus

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

Make rs397507939(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32362514

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507939
dbSNP (classic)	rs397507939
ClinGen	rs397507939
ebi	rs397507939
HLI	rs397507939
Exac	rs397507939
Gnomad	rs397507939
Varsome	rs397507939
LitVar	rs397507939
Map	rs397507939
PheGenI	rs397507939
Biobank	rs397507939
1000 genomes	rs397507939
hgdp	rs397507939
ensembl	rs397507939
geneview	rs397507939
scholar	rs397507939
google	rs397507939
pharmgkb	rs397507939
gwascentral	rs397507939
openSNP	rs397507939
23andMe	rs397507939
SNPshot	rs397507939
SNPdbe	rs397507939
MSV3d	rs397507939
GWAS Ctlg	rs397507939

Max Magnitude

6

ClinVar
Risk	rs397507939(G;G)
Alt	rs397507939(G;G)
Reference	Rs397507939(T;T)
Significance	Other
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.32936651T>G
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045323.2, RCV000113827.1,