rs81002796

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs81002796(G;T)

Make rs81002796(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32316528

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002796
dbSNP (classic)	rs81002796
ClinGen	rs81002796
ebi	rs81002796
HLI	rs81002796
Exac	rs81002796
Gnomad	rs81002796
Varsome	rs81002796
LitVar	rs81002796
Map	rs81002796
PheGenI	rs81002796
Biobank	rs81002796
1000 genomes	rs81002796
hgdp	rs81002796
ensembl	rs81002796
geneview	rs81002796
scholar	rs81002796
google	rs81002796
pharmgkb	rs81002796
gwascentral	rs81002796
openSNP	rs81002796
23andMe	rs81002796
SNPshot	rs81002796
SNPdbe	rs81002796
MSV3d	rs81002796
GWAS Ctlg	rs81002796

Max Magnitude

0

ClinVar
Risk	rs81002796(A;A) rs81002796(C;C) rs81002796(T;T)
Alt	rs81002796(A;A) rs81002796(C;C) rs81002796(T;T)
Reference	Rs81002796(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome Neoplasm of breast Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome Neoplasm of breast Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32890665G>A; NC_000013.10:g.32890665G>C; NC_000013.10:g.32890665G>T
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045021.2, RCV000077381.3, RCV000218090.1, RCV000217482.1, RCV000239221.1, RCV000240786.1, RCV000045022.3, RCV000077382.3, RCV000162894.1,