rs81002843

Orientation

plus

Stabilized

plus

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

Make rs81002843(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32356611

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002843
dbSNP (classic)	rs81002843
ClinGen	rs81002843
ebi	rs81002843
HLI	rs81002843
Exac	rs81002843
Gnomad	rs81002843
Varsome	rs81002843
LitVar	rs81002843
Map	rs81002843
PheGenI	rs81002843
Biobank	rs81002843
1000 genomes	rs81002843
hgdp	rs81002843
ensembl	rs81002843
geneview	rs81002843
scholar	rs81002843
google	rs81002843
pharmgkb	rs81002843
gwascentral	rs81002843
openSNP	rs81002843
23andMe	rs81002843
SNPshot	rs81002843
SNPdbe	rs81002843
MSV3d	rs81002843
GWAS Ctlg	rs81002843

Max Magnitude

6

ClinVar
Risk	rs81002843(G;G)
Alt	rs81002843(G;G)
Reference	Rs81002843(T;T)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32930748T>G
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045261.3, RCV000113793.1,