rs587781470

Orientation

plus

Stabilized

plus

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

Make rs587781470(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32340686

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587781470
dbSNP (classic)	rs587781470
ClinGen	rs587781470
ebi	rs587781470
HLI	rs587781470
Exac	rs587781470
Gnomad	rs587781470
Varsome	rs587781470
LitVar	rs587781470
Map	rs587781470
PheGenI	rs587781470
Biobank	rs587781470
1000 genomes	rs587781470
hgdp	rs587781470
ensembl	rs587781470
geneview	rs587781470
scholar	rs587781470
google	rs587781470
pharmgkb	rs587781470
gwascentral	rs587781470
openSNP	rs587781470
23andMe	rs587781470
SNPshot	rs587781470
SNPdbe	rs587781470
MSV3d	rs587781470
GWAS Ctlg	rs587781470

Max Magnitude

6

ClinVar
Risk	rs587781470(-;-)
Alt	rs587781470(-;-)
Reference	Rs587781470(AA;AA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32914823_32914824delAA
CLNSRC
CLNACC	RCV000129412.3, RCV000225411.2, RCV000484123.1,