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rs587781625

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781625(-;-)
Make rs587781625(-;A)
Make rs587781625(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132557418
GeneIL5, RAD50
is asnp
is mentioned by
dbSNPrs587781625
ebirs587781625
HLIrs587781625
Exacrs587781625
Varsomers587781625
Maprs587781625
PheGenIrs587781625
hapmaprs587781625
1000 genomesrs587781625
hgdprs587781625
ensemblrs587781625
gopubmedrs587781625
geneviewrs587781625
scholarrs587781625
googlers587781625
pharmgkbrs587781625
gwascentralrs587781625
openSNPrs587781625
23andMers587781625
23andMe allrs587781625
SNP Nexus

SNPshotrs587781625
SNPdbers587781625
MSV3drs587781625
GWAS Ctlgrs587781625
Max Magnitude0
ClinVar
Risk rs587781625(A;A)
Alt rs587781625(A;A)
Reference rs587781625(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50 IL5
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131893110dupA
CLNSRC
CLNACC RCV000129727.3,