rs398122762

Orientation

plus

Stabilized

plus

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

Make rs398122762(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337681

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122762
dbSNP (classic)	rs398122762
ClinGen	rs398122762
ebi	rs398122762
HLI	rs398122762
Exac	rs398122762
Gnomad	rs398122762
Varsome	rs398122762
LitVar	rs398122762
Map	rs398122762
PheGenI	rs398122762
Biobank	rs398122762
1000 genomes	rs398122762
hgdp	rs398122762
ensembl	rs398122762
geneview	rs398122762
scholar	rs398122762
google	rs398122762
pharmgkb	rs398122762
gwascentral	rs398122762
openSNP	rs398122762
23andMe	rs398122762
SNPshot	rs398122762
SNPdbe	rs398122762
MSV3d	rs398122762
GWAS Ctlg	rs398122762

Max Magnitude

6

ClinVar
Risk	rs398122762(-;-)
Alt	rs398122762(-;-)
Reference	Rs398122762(C;C)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911818delC
CLNSRC	ClinVar
CLNACC	RCV000077705.3,