rs81002831

Orientation

plus

Stabilized

plus

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

Make rs81002831(C;C)

Make rs81002831(C;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32330918

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002831
dbSNP (classic)	rs81002831
ClinGen	rs81002831
ebi	rs81002831
HLI	rs81002831
Exac	rs81002831
Gnomad	rs81002831
Varsome	rs81002831
LitVar	rs81002831
Map	rs81002831
PheGenI	rs81002831
Biobank	rs81002831
1000 genomes	rs81002831
hgdp	rs81002831
ensembl	rs81002831
geneview	rs81002831
scholar	rs81002831
google	rs81002831
pharmgkb	rs81002831
gwascentral	rs81002831
openSNP	rs81002831
23andMe	rs81002831
SNPshot	rs81002831
SNPdbe	rs81002831
MSV3d	rs81002831
GWAS Ctlg	rs81002831

Max Magnitude

6

ClinVar
Risk	rs81002831(C;C)
Alt	rs81002831(C;C)
Reference	Rs81002831(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32905055G>C
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045063.2, RCV000114011.1, RCV000215277.1,