rs587782613

Orientation

plus

Stabilized

plus

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

Make rs587782613(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32337767

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782613
dbSNP (classic)	rs587782613
ClinGen	rs587782613
ebi	rs587782613
HLI	rs587782613
Exac	rs587782613
Gnomad	rs587782613
Varsome	rs587782613
LitVar	rs587782613
Map	rs587782613
PheGenI	rs587782613
Biobank	rs587782613
1000 genomes	rs587782613
hgdp	rs587782613
ensembl	rs587782613
geneview	rs587782613
scholar	rs587782613
google	rs587782613
pharmgkb	rs587782613
gwascentral	rs587782613
openSNP	rs587782613
23andMe	rs587782613
SNPshot	rs587782613
SNPdbe	rs587782613
MSV3d	rs587782613
GWAS Ctlg	rs587782613

Max Magnitude

6

ClinVar
Risk	rs587782613(T;T)
Alt	rs587782613(T;T)
Reference	Rs587782613(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.32911904C>T
CLNSRC
CLNACC	RCV000131988.3, RCV000241121.2,