rs398122747

Orientation

plus

Stabilized

plus

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

Make rs398122747(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336725

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122747
dbSNP (classic)	rs398122747
ClinGen	rs398122747
ebi	rs398122747
HLI	rs398122747
Exac	rs398122747
Gnomad	rs398122747
Varsome	rs398122747
LitVar	rs398122747
Map	rs398122747
PheGenI	rs398122747
Biobank	rs398122747
1000 genomes	rs398122747
hgdp	rs398122747
ensembl	rs398122747
geneview	rs398122747
scholar	rs398122747
google	rs398122747
pharmgkb	rs398122747
gwascentral	rs398122747
openSNP	rs398122747
23andMe	rs398122747
SNPshot	rs398122747
SNPdbe	rs398122747
MSV3d	rs398122747
GWAS Ctlg	rs398122747

Max Magnitude

6

ClinVar
Risk	rs398122747(-;-)
Alt	rs398122747(-;-)
Reference	Rs398122747(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910862delA
CLNSRC	ClinVar
CLNACC	RCV000077685.3,