rs398122531

Orientation

plus

Stabilized

plus

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

Make rs398122531(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339707

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122531
dbSNP (classic)	rs398122531
ClinGen	rs398122531
ebi	rs398122531
HLI	rs398122531
Exac	rs398122531
Gnomad	rs398122531
Varsome	rs398122531
LitVar	rs398122531
Map	rs398122531
PheGenI	rs398122531
Biobank	rs398122531
1000 genomes	rs398122531
hgdp	rs398122531
ensembl	rs398122531
geneview	rs398122531
scholar	rs398122531
google	rs398122531
pharmgkb	rs398122531
gwascentral	rs398122531
openSNP	rs398122531
23andMe	rs398122531
SNPshot	rs398122531
SNPdbe	rs398122531
MSV3d	rs398122531
GWAS Ctlg	rs398122531

Max Magnitude

6

ClinVar
Risk	rs398122531(-;-)
Alt	rs398122531(-;-)
Reference	Rs398122531(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.32913844delC
CLNSRC	ClinVar
CLNACC	RCV000076930.4,