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rs587781721

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781721(-;-)
Make rs587781721(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132575917
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781721
ebirs587781721
HLIrs587781721
Exacrs587781721
Varsomers587781721
Maprs587781721
PheGenIrs587781721
hapmaprs587781721
1000 genomesrs587781721
hgdprs587781721
ensemblrs587781721
gopubmedrs587781721
geneviewrs587781721
scholarrs587781721
googlers587781721
pharmgkbrs587781721
gwascentralrs587781721
openSNPrs587781721
23andMers587781721
23andMe allrs587781721
SNP Nexus

SNPshotrs587781721
SNPdbers587781721
MSV3drs587781721
GWAS Ctlgrs587781721
Max Magnitude0
ClinVar
Risk rs587781721(;)
Alt rs587781721(;)
Reference rs587781721(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131911609delT
CLNSRC
CLNACC RCV000129908.2,