rs431825343

Orientation

plus

Stabilized

plus

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

Make rs431825343(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340957

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs431825343
dbSNP (classic)	rs431825343
ClinGen	rs431825343
ebi	rs431825343
HLI	rs431825343
Exac	rs431825343
Gnomad	rs431825343
Varsome	rs431825343
LitVar	rs431825343
Map	rs431825343
PheGenI	rs431825343
Biobank	rs431825343
1000 genomes	rs431825343
hgdp	rs431825343
ensembl	rs431825343
geneview	rs431825343
scholar	rs431825343
google	rs431825343
pharmgkb	rs431825343
gwascentral	rs431825343
openSNP	rs431825343
23andMe	rs431825343
SNPshot	rs431825343
SNPdbe	rs431825343
MSV3d	rs431825343
GWAS Ctlg	rs431825343

Max Magnitude

6

ClinVar
Risk	rs431825343(-;-)
Alt	rs431825343(-;-)
Reference	Rs431825343(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.32915094delC
CLNSRC	ClinVar
CLNACC	RCV000082960.4,