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rs587781327

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs587781327(-;-)
Make rs587781327(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132589653
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781327
ebirs587781327
HLIrs587781327
Exacrs587781327
Varsomers587781327
Maprs587781327
PheGenIrs587781327
hapmaprs587781327
1000 genomesrs587781327
hgdprs587781327
ensemblrs587781327
gopubmedrs587781327
geneviewrs587781327
scholarrs587781327
googlers587781327
pharmgkbrs587781327
gwascentralrs587781327
openSNPrs587781327
23andMers587781327
23andMe allrs587781327
SNP Nexus

SNPshotrs587781327
SNPdbers587781327
MSV3drs587781327
GWAS Ctlgrs587781327
Max Magnitude0
ClinVar
Risk rs587781327(;)
Alt rs587781327(;)
Reference rs587781327(CT;CT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131925347_131925348delCT
CLNSRC
CLNACC RCV000167173.4,