rs398122612

Orientation

plus

Stabilized

plus

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

Make rs398122612(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394808

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122612
dbSNP (classic)	rs398122612
ClinGen	rs398122612
ebi	rs398122612
HLI	rs398122612
Exac	rs398122612
Gnomad	rs398122612
Varsome	rs398122612
LitVar	rs398122612
Map	rs398122612
PheGenI	rs398122612
Biobank	rs398122612
1000 genomes	rs398122612
hgdp	rs398122612
ensembl	rs398122612
geneview	rs398122612
scholar	rs398122612
google	rs398122612
pharmgkb	rs398122612
gwascentral	rs398122612
openSNP	rs398122612
23andMe	rs398122612
SNPshot	rs398122612
SNPdbe	rs398122612
MSV3d	rs398122612
GWAS Ctlg	rs398122612

Max Magnitude

6

ClinVar
Risk	rs398122612(-;-)
Alt	rs398122612(-;-)
Reference	Rs398122612(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.32968945delC
CLNSRC	ClinVar
CLNACC	RCV000077040.3,