rs587781585

Orientation

plus

Stabilized

plus

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

Make rs587781585(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32339777

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587781585
dbSNP (classic)	rs587781585
ClinGen	rs587781585
ebi	rs587781585
HLI	rs587781585
Exac	rs587781585
Gnomad	rs587781585
Varsome	rs587781585
LitVar	rs587781585
Map	rs587781585
PheGenI	rs587781585
Biobank	rs587781585
1000 genomes	rs587781585
hgdp	rs587781585
ensembl	rs587781585
geneview	rs587781585
scholar	rs587781585
google	rs587781585
pharmgkb	rs587781585
gwascentral	rs587781585
openSNP	rs587781585
23andMe	rs587781585
SNPshot	rs587781585
SNPdbe	rs587781585
MSV3d	rs587781585
GWAS Ctlg	rs587781585

Max Magnitude

6

ClinVar
Risk	rs587781585(-;-)
Alt	rs587781585(-;-)
Reference	Rs587781585(AT;AT)
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.32913914_32913915delAT
CLNSRC
CLNACC	RCV000129625.2, RCV000241292.1,