Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781470

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587781470(-;-)
Make rs587781470(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32340686
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781470
ebirs587781470
HLIrs587781470
Exacrs587781470
Varsomers587781470
Maprs587781470
PheGenIrs587781470
hapmaprs587781470
1000 genomesrs587781470
hgdprs587781470
ensemblrs587781470
gopubmedrs587781470
geneviewrs587781470
scholarrs587781470
googlers587781470
pharmgkbrs587781470
gwascentralrs587781470
openSNPrs587781470
23andMers587781470
23andMe allrs587781470
SNP Nexus

SNPshotrs587781470
SNPdbers587781470
MSV3drs587781470
GWAS Ctlgrs587781470
Max Magnitude0
ClinVar
Risk rs587781470(;)
Alt rs587781470(;)
Reference rs587781470(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.32914823_32914824delAA
CLNSRC
CLNACC RCV000129412.2, RCV000225411.1,