rs431825321

Orientation

plus

Stabilized

plus

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

Make rs431825321(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338874

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs431825321
dbSNP (classic)	rs431825321
ClinGen	rs431825321
ebi	rs431825321
HLI	rs431825321
Exac	rs431825321
Gnomad	rs431825321
Varsome	rs431825321
LitVar	rs431825321
Map	rs431825321
PheGenI	rs431825321
Biobank	rs431825321
1000 genomes	rs431825321
hgdp	rs431825321
ensembl	rs431825321
geneview	rs431825321
scholar	rs431825321
google	rs431825321
pharmgkb	rs431825321
gwascentral	rs431825321
openSNP	rs431825321
23andMe	rs431825321
SNPshot	rs431825321
SNPdbe	rs431825321
MSV3d	rs431825321
GWAS Ctlg	rs431825321

Max Magnitude

6

ClinVar
Risk	rs431825321(-;-)
Alt	rs431825321(-;-)
Reference	Rs431825321(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.32913011delC
CLNSRC	ClinVar
CLNACC	RCV000082929.4,