rs81002883

Orientation

plus

Stabilized

plus

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

Make rs81002883(A;A)

Make rs81002883(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32380146

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002883
dbSNP (classic)	rs81002883
ClinGen	rs81002883
ebi	rs81002883
HLI	rs81002883
Exac	rs81002883
Gnomad	rs81002883
Varsome	rs81002883
LitVar	rs81002883
Map	rs81002883
PheGenI	rs81002883
Biobank	rs81002883
1000 genomes	rs81002883
hgdp	rs81002883
ensembl	rs81002883
geneview	rs81002883
scholar	rs81002883
google	rs81002883
pharmgkb	rs81002883
gwascentral	rs81002883
openSNP	rs81002883
23andMe	rs81002883
SNPshot	rs81002883
SNPdbe	rs81002883
MSV3d	rs81002883
GWAS Ctlg	rs81002883

Max Magnitude

6

ClinVar
Risk	rs81002883(A;A) rs81002883(C;C)
Alt	rs81002883(A;A) rs81002883(C;C)
Reference	Rs81002883(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32954283G>A; NC_000013.10:g.32954283G>C
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045761.2, RCV000114075.1, RCV000083002.2,