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rs587781355

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs587781355(-;-)
Make rs587781355(-;TG)
Make rs587781355(TG;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132579350
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781355
ebirs587781355
HLIrs587781355
Exacrs587781355
Varsomers587781355
Maprs587781355
PheGenIrs587781355
hapmaprs587781355
1000 genomesrs587781355
hgdprs587781355
ensemblrs587781355
gopubmedrs587781355
geneviewrs587781355
scholarrs587781355
googlers587781355
pharmgkbrs587781355
gwascentralrs587781355
openSNPrs587781355
23andMers587781355
23andMe allrs587781355
SNP Nexus

SNPshotrs587781355
SNPdbers587781355
MSV3drs587781355
GWAS Ctlgrs587781355
Max Magnitude0
ClinVar
Risk rs587781355(;)
Alt rs587781355(;)
Reference rs587781355(GT;GT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131915042_131915043delTG
CLNSRC
CLNACC RCV000129139.3,