rs81002836

Orientation

plus

Stabilized

plus

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

Make rs81002836(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32362521

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002836
dbSNP (classic)	rs81002836
ClinGen	rs81002836
ebi	rs81002836
HLI	rs81002836
Exac	rs81002836
Gnomad	rs81002836
Varsome	rs81002836
LitVar	rs81002836
Map	rs81002836
PheGenI	rs81002836
Biobank	rs81002836
1000 genomes	rs81002836
hgdp	rs81002836
ensembl	rs81002836
geneview	rs81002836
scholar	rs81002836
google	rs81002836
pharmgkb	rs81002836
gwascentral	rs81002836
openSNP	rs81002836
23andMe	rs81002836
SNPshot	rs81002836
SNPdbe	rs81002836
MSV3d	rs81002836
GWAS Ctlg	rs81002836

Max Magnitude

6

ClinVar
Risk	rs81002836(G;G) rs81002836(T;T)
Alt	rs81002836(G;G) rs81002836(T;T)
Reference	Rs81002836(A;A)
Significance	Other
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome Ovarian neoplasm
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Ovarian neoplasm
Reversed	0
HGVS	NC_000013.10:g.32936658A>G; NC_000013.10:g.32936658A>T
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045321.3, RCV000077414.4, RCV000131088.3, RCV000414989.1, RCV000258419.1,