rs587782605

Orientation

plus

Stabilized

plus

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

Make rs587782605(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32339825

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782605
dbSNP (classic)	rs587782605
ClinGen	rs587782605
ebi	rs587782605
HLI	rs587782605
Exac	rs587782605
Gnomad	rs587782605
Varsome	rs587782605
LitVar	rs587782605
Map	rs587782605
PheGenI	rs587782605
Biobank	rs587782605
1000 genomes	rs587782605
hgdp	rs587782605
ensembl	rs587782605
geneview	rs587782605
scholar	rs587782605
google	rs587782605
pharmgkb	rs587782605
gwascentral	rs587782605
openSNP	rs587782605
23andMe	rs587782605
SNPshot	rs587782605
SNPdbe	rs587782605
MSV3d	rs587782605
GWAS Ctlg	rs587782605

Max Magnitude

6

ClinVar
Risk	rs587782605(-;-)
Alt	rs587782605(-;-)
Reference	Rs587782605(AA;AA)
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.32913962_32913963delAA
CLNSRC
CLNACC	RCV000131974.2, RCV000241399.1,