rs397507867

Orientation

plus

Stabilized

plus

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

Make rs397507867(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340912

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507867
dbSNP (classic)	rs397507867
ClinGen	rs397507867
ebi	rs397507867
HLI	rs397507867
Exac	rs397507867
Gnomad	rs397507867
Varsome	rs397507867
LitVar	rs397507867
Map	rs397507867
PheGenI	rs397507867
Biobank	rs397507867
1000 genomes	rs397507867
hgdp	rs397507867
ensembl	rs397507867
geneview	rs397507867
scholar	rs397507867
google	rs397507867
pharmgkb	rs397507867
gwascentral	rs397507867
openSNP	rs397507867
23andMe	rs397507867
SNPshot	rs397507867
SNPdbe	rs397507867
MSV3d	rs397507867
GWAS Ctlg	rs397507867

Max Magnitude

6

ClinVar
Risk	rs397507867(A;A) rs397507867(G;G) rs397507867(T;T)
Alt	rs397507867(A;A) rs397507867(G;G) rs397507867(T;T)
Reference	Rs397507867(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32915049C>A; NC_000013.10:g.32915049C>G; NC_000013.10:g.32915049C>T
CLNSRC	ClinVar
CLNACC	RCV000044984.2, RCV000241520.2, RCV000257527.2, RCV000475735.1,