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rs587781930

From SNPedia

Orientationplus
Geno Mag Summary
(AATC;AATC) 0 common in clinvar
Make rs587781930(-;-)
Make rs587781930(-;TCAA)
Make rs587781930(TCAA;TCAA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132608685
GeneRAD50
is asnp
is mentioned by
dbSNPrs587781930
ebirs587781930
HLIrs587781930
Exacrs587781930
Varsomers587781930
Maprs587781930
PheGenIrs587781930
hapmaprs587781930
1000 genomesrs587781930
hgdprs587781930
ensemblrs587781930
gopubmedrs587781930
geneviewrs587781930
scholarrs587781930
googlers587781930
pharmgkbrs587781930
gwascentralrs587781930
openSNPrs587781930
23andMers587781930
23andMe allrs587781930
SNP Nexus

SNPshotrs587781930
SNPdbers587781930
MSV3drs587781930
GWAS Ctlgrs587781930
Max Magnitude0
ClinVar
Risk rs587781930(;)
Alt rs587781930(;)
Reference rs587781930(AATC;AATC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131944377_131944380delTCAA
CLNSRC
CLNACC RCV000130289.2,