rs587782667

Orientation

plus

Stabilized

plus

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

Make rs587782667(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32341058

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs587782667
dbSNP (classic)	rs587782667
ClinGen	rs587782667
ebi	rs587782667
HLI	rs587782667
Exac	rs587782667
Gnomad	rs587782667
Varsome	rs587782667
LitVar	rs587782667
Map	rs587782667
PheGenI	rs587782667
Biobank	rs587782667
1000 genomes	rs587782667
hgdp	rs587782667
ensembl	rs587782667
geneview	rs587782667
scholar	rs587782667
google	rs587782667
pharmgkb	rs587782667
gwascentral	rs587782667
openSNP	rs587782667
23andMe	rs587782667
SNPshot	rs587782667
SNPdbe	rs587782667
MSV3d	rs587782667
GWAS Ctlg	rs587782667

Max Magnitude

6

ClinVar
Risk	rs587782667(-;-)
Alt	rs587782667(-;-)
Reference	Rs587782667(TA;TA)
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.32915195_32915196delAT
CLNSRC
CLNACC	RCV000132088.2, RCV000241108.1,