rs587780651

Merged into

rs431825312

Orientation

plus

Stabilized

plus

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

Make rs587780651(-;-)

Make rs587780651(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32338132

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587780651
dbSNP (classic)	rs587780651
ClinGen	rs587780651
ebi	rs587780651
HLI	rs587780651
Exac	rs587780651
Gnomad	rs587780651
Varsome	rs587780651
LitVar	rs587780651
Map	rs587780651
PheGenI	rs587780651
Biobank	rs587780651
1000 genomes	rs587780651
hgdp	rs587780651
ensembl	rs587780651
geneview	rs587780651
scholar	rs587780651
google	rs587780651
pharmgkb	rs587780651
gwascentral	rs587780651
openSNP	rs587780651
23andMe	rs587780651
SNPshot	rs587780651
SNPdbe	rs587780651
MSV3d	rs587780651
GWAS Ctlg	rs587780651

Status

Merged into rs431825312

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs587780651(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32912271delT
CLNSRC
CLNACC	RCV000082919.4, RCV000122909.1,