rs431825332

Orientation

plus

Stabilized

plus

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

Make rs431825332(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339933

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs431825332
dbSNP (classic)	rs431825332
ClinGen	rs431825332
ebi	rs431825332
HLI	rs431825332
Exac	rs431825332
Gnomad	rs431825332
Varsome	rs431825332
LitVar	rs431825332
Map	rs431825332
PheGenI	rs431825332
Biobank	rs431825332
1000 genomes	rs431825332
hgdp	rs431825332
ensembl	rs431825332
geneview	rs431825332
scholar	rs431825332
google	rs431825332
pharmgkb	rs431825332
gwascentral	rs431825332
openSNP	rs431825332
23andMe	rs431825332
SNPshot	rs431825332
SNPdbe	rs431825332
MSV3d	rs431825332
GWAS Ctlg	rs431825332

Max Magnitude

6

ClinVar
Risk	rs431825332(T;T)
Alt	rs431825332(T;T)
Reference	Rs431825332(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32914070A>T
CLNSRC	ClinVar
CLNACC	RCV000082944.3, RCV000164633.1,