rs587782010

Orientation

plus

Stabilized

plus

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

Make rs587782010(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32371076

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782010
dbSNP (classic)	rs587782010
ClinGen	rs587782010
ebi	rs587782010
HLI	rs587782010
Exac	rs587782010
Gnomad	rs587782010
Varsome	rs587782010
LitVar	rs587782010
Map	rs587782010
PheGenI	rs587782010
Biobank	rs587782010
1000 genomes	rs587782010
hgdp	rs587782010
ensembl	rs587782010
geneview	rs587782010
scholar	rs587782010
google	rs587782010
pharmgkb	rs587782010
gwascentral	rs587782010
openSNP	rs587782010
23andMe	rs587782010
SNPshot	rs587782010
SNPdbe	rs587782010
MSV3d	rs587782010
GWAS Ctlg	rs587782010

Max Magnitude

6

ClinVar
Risk	rs587782010(T;T)
Alt	rs587782010(T;T)
Reference	Rs587782010(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32945213C>T
CLNSRC
CLNACC	RCV000130433.2, RCV000241135.1,