rs397507649

Orientation

plus

Stabilized

plus

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

Make rs397507649(A;A)

Make rs397507649(A;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337345

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507649
dbSNP (classic)	rs397507649
ClinGen	rs397507649
ebi	rs397507649
HLI	rs397507649
Exac	rs397507649
Gnomad	rs397507649
Varsome	rs397507649
LitVar	rs397507649
Map	rs397507649
PheGenI	rs397507649
Biobank	rs397507649
1000 genomes	rs397507649
hgdp	rs397507649
ensembl	rs397507649
geneview	rs397507649
scholar	rs397507649
google	rs397507649
pharmgkb	rs397507649
gwascentral	rs397507649
openSNP	rs397507649
23andMe	rs397507649
SNPshot	rs397507649
SNPdbe	rs397507649
MSV3d	rs397507649
GWAS Ctlg	rs397507649

Max Magnitude

6

ClinVar
Risk	rs397507649(A;A) rs397507649(G;G)
Alt	rs397507649(A;A) rs397507649(G;G)
Reference	Rs397507649(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.32911482T>A; NC_000013.10:g.32911482T>G
CLNSRC	ClinVar
CLNACC	RCV000044100.2, RCV000256883.2,