rs587782780

Orientation

plus

Stabilized

plus

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

Make rs587782780(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32336414

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782780
dbSNP (classic)	rs587782780
ClinGen	rs587782780
ebi	rs587782780
HLI	rs587782780
Exac	rs587782780
Gnomad	rs587782780
Varsome	rs587782780
LitVar	rs587782780
Map	rs587782780
PheGenI	rs587782780
Biobank	rs587782780
1000 genomes	rs587782780
hgdp	rs587782780
ensembl	rs587782780
geneview	rs587782780
scholar	rs587782780
google	rs587782780
pharmgkb	rs587782780
gwascentral	rs587782780
openSNP	rs587782780
23andMe	rs587782780
SNPshot	rs587782780
SNPdbe	rs587782780
MSV3d	rs587782780
GWAS Ctlg	rs587782780

Max Magnitude

6

ClinVar
Risk	rs587782780(-;-)
Alt	rs587782780(-;-)
Reference	Rs587782780(GATTA;GATTA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Neoplasm of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Neoplasm of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910551_32910555delGATTA
CLNSRC
CLNACC	RCV000132320.2, RCV000240749.1, RCV000241369.1,