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rs587782895

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587782895(-;-)
Make rs587782895(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132604020
GeneRAD50
is asnp
is mentioned by
dbSNPrs587782895
ebirs587782895
HLIrs587782895
Exacrs587782895
Varsomers587782895
Maprs587782895
PheGenIrs587782895
hapmaprs587782895
1000 genomesrs587782895
hgdprs587782895
ensemblrs587782895
gopubmedrs587782895
geneviewrs587782895
scholarrs587782895
googlers587782895
pharmgkbrs587782895
gwascentralrs587782895
openSNPrs587782895
23andMers587782895
23andMe allrs587782895
SNP Nexus

SNPshotrs587782895
SNPdbers587782895
MSV3drs587782895
GWAS Ctlgrs587782895
Max Magnitude0
ClinVar
Risk rs587782895(;)
Alt rs587782895(;)
Reference rs587782895(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131939712_131939713delAA
CLNSRC
CLNACC RCV000132534.2,