rs81002893

Orientation

plus

Stabilized

plus

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

Make rs81002893(A;G)

Make rs81002893(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32376795

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002893
dbSNP (classic)	rs81002893
ClinGen	rs81002893
ebi	rs81002893
HLI	rs81002893
Exac	rs81002893
Gnomad	rs81002893
Varsome	rs81002893
LitVar	rs81002893
Map	rs81002893
PheGenI	rs81002893
Biobank	rs81002893
1000 genomes	rs81002893
hgdp	rs81002893
ensembl	rs81002893
geneview	rs81002893
scholar	rs81002893
google	rs81002893
pharmgkb	rs81002893
gwascentral	rs81002893
openSNP	rs81002893
23andMe	rs81002893
SNPshot	rs81002893
SNPdbe	rs81002893
MSV3d	rs81002893
GWAS Ctlg	rs81002893

Max Magnitude

0

ClinVar
Risk	rs81002893(G;G) rs81002893(T;T)
Alt	rs81002893(G;G) rs81002893(T;T)
Reference	Rs81002893(A;A)
Significance	Other
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32950932A>G; NC_000013.10:g.32950932A>T
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045615.2, RCV000077450.6, RCV000204178.1, RCV000410920.1,