rs587782901

Orientation

plus

Stabilized

plus

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

Make rs587782901(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32340070

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782901
dbSNP (classic)	rs587782901
ClinGen	rs587782901
ebi	rs587782901
HLI	rs587782901
Exac	rs587782901
Gnomad	rs587782901
Varsome	rs587782901
LitVar	rs587782901
Map	rs587782901
PheGenI	rs587782901
Biobank	rs587782901
1000 genomes	rs587782901
hgdp	rs587782901
ensembl	rs587782901
geneview	rs587782901
scholar	rs587782901
google	rs587782901
pharmgkb	rs587782901
gwascentral	rs587782901
openSNP	rs587782901
23andMe	rs587782901
SNPshot	rs587782901
SNPdbe	rs587782901
MSV3d	rs587782901
GWAS Ctlg	rs587782901

Max Magnitude

6

ClinVar
Risk	rs587782901(T;T)
Alt	rs587782901(T;T)
Reference	Rs587782901(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32914207dupT
CLNSRC
CLNACC	RCV000132544.3, RCV000239079.2, RCV000466847.1,