rs398122715

Orientation

plus

Stabilized

plus

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

Make rs398122715(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379401

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122715
dbSNP (classic)	rs398122715
ClinGen	rs398122715
ebi	rs398122715
HLI	rs398122715
Exac	rs398122715
Gnomad	rs398122715
Varsome	rs398122715
LitVar	rs398122715
Map	rs398122715
PheGenI	rs398122715
Biobank	rs398122715
1000 genomes	rs398122715
hgdp	rs398122715
ensembl	rs398122715
geneview	rs398122715
scholar	rs398122715
google	rs398122715
pharmgkb	rs398122715
gwascentral	rs398122715
openSNP	rs398122715
23andMe	rs398122715
SNPshot	rs398122715
SNPdbe	rs398122715
MSV3d	rs398122715
GWAS Ctlg	rs398122715

Max Magnitude

6

ClinVar
Risk	rs398122715(T;T)
Alt	rs398122715(T;T)
Reference	Rs398122715(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32953538G>T
CLNSRC	ClinVar
CLNACC	RCV000077644.4, RCV000198305.2,