rs81002795

Orientation

plus

Stabilized

plus

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

Make rs81002795(A;T)

Make rs81002795(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326153

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002795
dbSNP (classic)	rs81002795
ClinGen	rs81002795
ebi	rs81002795
HLI	rs81002795
Exac	rs81002795
Gnomad	rs81002795
Varsome	rs81002795
LitVar	rs81002795
Map	rs81002795
PheGenI	rs81002795
Biobank	rs81002795
1000 genomes	rs81002795
hgdp	rs81002795
ensembl	rs81002795
geneview	rs81002795
scholar	rs81002795
google	rs81002795
pharmgkb	rs81002795
gwascentral	rs81002795
openSNP	rs81002795
23andMe	rs81002795
SNPshot	rs81002795
SNPdbe	rs81002795
MSV3d	rs81002795
GWAS Ctlg	rs81002795

Max Magnitude

0

ClinVar
Risk	rs81002795(G;G) rs81002795(T;T)
Alt	rs81002795(G;G) rs81002795(T;T)
Reference	Rs81002795(A;A)
Significance	Other
Disease	Familial cancer of breast Breast-ovarian cancer not specified
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not specified
Reversed	0
HGVS	NC_000013.10:g.32900290A>G; NC_000013.10:g.32900290A>T
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044484.2, RCV000258385.1, RCV000479466.1, RCV000113646.1,