rs397507663

Orientation

plus

Stabilized

plus

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

Make rs397507663(C;G)

Make rs397507663(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337651

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507663
dbSNP (classic)	rs397507663
ClinGen	rs397507663
ebi	rs397507663
HLI	rs397507663
Exac	rs397507663
Gnomad	rs397507663
Varsome	rs397507663
LitVar	rs397507663
Map	rs397507663
PheGenI	rs397507663
Biobank	rs397507663
1000 genomes	rs397507663
hgdp	rs397507663
ensembl	rs397507663
geneview	rs397507663
scholar	rs397507663
google	rs397507663
pharmgkb	rs397507663
gwascentral	rs397507663
openSNP	rs397507663
23andMe	rs397507663
SNPshot	rs397507663
SNPdbe	rs397507663
MSV3d	rs397507663
GWAS Ctlg	rs397507663

Max Magnitude

6

ClinVar
Risk	rs397507663(A;A) rs397507663(G;G)
Alt	rs397507663(A;A) rs397507663(G;G)
Reference	Rs397507663(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32911788C>A; NC_000013.10:g.32911788C>G
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000131361.2, RCV000241055.2, RCV000044172.2,