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rs587776467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776467(-;-)
Make rs587776467(-;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position32339741
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587776467
ebirs587776467
HLIrs587776467
Exacrs587776467
Varsomers587776467
Maprs587776467
PheGenIrs587776467
hapmaprs587776467
1000 genomesrs587776467
hgdprs587776467
ensemblrs587776467
gopubmedrs587776467
geneviewrs587776467
scholarrs587776467
googlers587776467
pharmgkbrs587776467
gwascentralrs587776467
openSNPrs587776467
23andMers587776467
23andMe allrs587776467
SNP Nexus

SNPshotrs587776467
SNPdbers587776467
MSV3drs587776467
GWAS Ctlgrs587776467
Max Magnitude0
ClinVar
Risk rs587776467(;)
Alt rs587776467(;)
Reference rs587776467(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913878delG
CLNSRC ClinVar
CLNACC RCV000144188.1,