rs81002895

Orientation

plus

Stabilized

plus

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

Make rs81002895(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32398160

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002895
dbSNP (classic)	rs81002895
ClinGen	rs81002895
ebi	rs81002895
HLI	rs81002895
Exac	rs81002895
Gnomad	rs81002895
Varsome	rs81002895
LitVar	rs81002895
Map	rs81002895
PheGenI	rs81002895
Biobank	rs81002895
1000 genomes	rs81002895
hgdp	rs81002895
ensembl	rs81002895
geneview	rs81002895
scholar	rs81002895
google	rs81002895
pharmgkb	rs81002895
gwascentral	rs81002895
openSNP	rs81002895
23andMe	rs81002895
SNPshot	rs81002895
SNPdbe	rs81002895
MSV3d	rs81002895
GWAS Ctlg	rs81002895

Max Magnitude

6

ClinVar
Risk	rs81002895(G;G)
Alt	rs81002895(G;G)
Reference	Rs81002895(A;A)
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.32972297A>G
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045879.2, RCV000114145.1,