rs398122737

Orientation

plus

Stabilized

plus

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

Make rs398122737(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336380

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122737
dbSNP (classic)	rs398122737
ClinGen	rs398122737
ebi	rs398122737
HLI	rs398122737
Exac	rs398122737
Gnomad	rs398122737
Varsome	rs398122737
LitVar	rs398122737
Map	rs398122737
PheGenI	rs398122737
Biobank	rs398122737
1000 genomes	rs398122737
hgdp	rs398122737
ensembl	rs398122737
geneview	rs398122737
scholar	rs398122737
google	rs398122737
pharmgkb	rs398122737
gwascentral	rs398122737
openSNP	rs398122737
23andMe	rs398122737
SNPshot	rs398122737
SNPdbe	rs398122737
MSV3d	rs398122737
GWAS Ctlg	rs398122737

Max Magnitude

6

ClinVar
Risk	rs398122737(-;-)
Alt	rs398122737(-;-)
Reference	Rs398122737(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.32910517delA
CLNSRC	ClinVar
CLNACC	RCV000077674.3,