rs397507719

Orientation

plus

Stabilized

plus

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

Make rs397507719(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338795

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507719
dbSNP (classic)	rs397507719
ClinGen	rs397507719
ebi	rs397507719
HLI	rs397507719
Exac	rs397507719
Gnomad	rs397507719
Varsome	rs397507719
LitVar	rs397507719
Map	rs397507719
PheGenI	rs397507719
Biobank	rs397507719
1000 genomes	rs397507719
hgdp	rs397507719
ensembl	rs397507719
geneview	rs397507719
scholar	rs397507719
google	rs397507719
pharmgkb	rs397507719
gwascentral	rs397507719
openSNP	rs397507719
23andMe	rs397507719
SNPshot	rs397507719
SNPdbe	rs397507719
MSV3d	rs397507719
GWAS Ctlg	rs397507719

Max Magnitude

6

ClinVar
Risk	rs397507719(C;C) rs397507719(G;G)
Alt	rs397507719(C;C) rs397507719(G;G)
Reference	Rs397507719(T;T)
Significance	Pathogenic
Disease	not specified Familial cancer of breast not provided Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	not specified Familial cancer of breast not provided Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912932T>C; NC_000013.10:g.32912932T>G
CLNSRC	ClinVar
CLNACC	RCV000435177.1, RCV000044415.2, RCV000222409.1, RCV000225483.2,