rs81002802

Orientation

plus

Stabilized

plus

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

Make rs81002802(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379914

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002802
dbSNP (classic)	rs81002802
ClinGen	rs81002802
ebi	rs81002802
HLI	rs81002802
Exac	rs81002802
Gnomad	rs81002802
Varsome	rs81002802
LitVar	rs81002802
Map	rs81002802
PheGenI	rs81002802
Biobank	rs81002802
1000 genomes	rs81002802
hgdp	rs81002802
ensembl	rs81002802
geneview	rs81002802
scholar	rs81002802
google	rs81002802
pharmgkb	rs81002802
gwascentral	rs81002802
openSNP	rs81002802
23andMe	rs81002802
SNPshot	rs81002802
SNPdbe	rs81002802
MSV3d	rs81002802
GWAS Ctlg	rs81002802

Max Magnitude

6

ClinVar
Risk	rs81002802(A;A) rs81002802(T;T)
Alt	rs81002802(A;A) rs81002802(T;T)
Reference	Rs81002802(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.32954051G>A; NC_000013.10:g.32954051G>T
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045721.2, RCV000114050.2, RCV000045722.2, RCV000114051.1,