rs431825338

Orientation

plus

Stabilized

plus

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

Make rs431825338(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340566

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs431825338
dbSNP (classic)	rs431825338
ClinGen	rs431825338
ebi	rs431825338
HLI	rs431825338
Exac	rs431825338
Gnomad	rs431825338
Varsome	rs431825338
LitVar	rs431825338
Map	rs431825338
PheGenI	rs431825338
Biobank	rs431825338
1000 genomes	rs431825338
hgdp	rs431825338
ensembl	rs431825338
geneview	rs431825338
scholar	rs431825338
google	rs431825338
pharmgkb	rs431825338
gwascentral	rs431825338
openSNP	rs431825338
23andMe	rs431825338
SNPshot	rs431825338
SNPdbe	rs431825338
MSV3d	rs431825338
GWAS Ctlg	rs431825338

Max Magnitude

6

ClinVar
Risk	rs431825338(-;-)
Alt	rs431825338(-;-)
Reference	Rs431825338(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer not specified
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not specified
Reversed	0
HGVS	NC_000013.10:g.32914703delA
CLNSRC	ClinVar
CLNACC	RCV000082955.3, RCV000238665.1,