rs397508028

Orientation

plus

Stabilized

plus

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

Make rs397508028(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379787

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508028
dbSNP (classic)	rs397508028
ClinGen	rs397508028
ebi	rs397508028
HLI	rs397508028
Exac	rs397508028
Gnomad	rs397508028
Varsome	rs397508028
LitVar	rs397508028
Map	rs397508028
PheGenI	rs397508028
Biobank	rs397508028
1000 genomes	rs397508028
hgdp	rs397508028
ensembl	rs397508028
geneview	rs397508028
scholar	rs397508028
google	rs397508028
pharmgkb	rs397508028
gwascentral	rs397508028
openSNP	rs397508028
23andMe	rs397508028
SNPshot	rs397508028
SNPdbe	rs397508028
MSV3d	rs397508028
GWAS Ctlg	rs397508028

Max Magnitude

6

ClinVar
Risk	rs397508028(G;G)
Alt	rs397508028(G;G)
Reference	Rs397508028(T;T)
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.32953924T>G
CLNSRC	ClinVar
CLNACC	RCV000045682.2, RCV000257890.2,