rs398122557

Orientation

plus

Stabilized

plus

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

Make rs398122557(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340799

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122557
dbSNP (classic)	rs398122557
ClinGen	rs398122557
ebi	rs398122557
HLI	rs398122557
Exac	rs398122557
Gnomad	rs398122557
Varsome	rs398122557
LitVar	rs398122557
Map	rs398122557
PheGenI	rs398122557
Biobank	rs398122557
1000 genomes	rs398122557
hgdp	rs398122557
ensembl	rs398122557
geneview	rs398122557
scholar	rs398122557
google	rs398122557
pharmgkb	rs398122557
gwascentral	rs398122557
openSNP	rs398122557
23andMe	rs398122557
SNPshot	rs398122557
SNPdbe	rs398122557
MSV3d	rs398122557
GWAS Ctlg	rs398122557

Max Magnitude

6

ClinVar
Risk	rs398122557(-;-)
Alt	rs398122557(-;-)
Reference	Rs398122557(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914936delT
CLNSRC	ClinVar
CLNACC	RCV000076966.4,