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rs1060501942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AACTT;AACTT) 0 common in clinvar
Make rs1060501942(-;-)
Make rs1060501942(-;CTTAA)
Make rs1060501942(CTTAA;CTTAA)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132609298
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501942
dbSNP (classic)rs1060501942
ClinGenrs1060501942
ebirs1060501942
HLIrs1060501942
Exacrs1060501942
Gnomadrs1060501942
Varsomers1060501942
LitVarrs1060501942
Maprs1060501942
PheGenIrs1060501942
Biobankrs1060501942
1000 genomesrs1060501942
hgdprs1060501942
ensemblrs1060501942
geneviewrs1060501942
scholarrs1060501942
googlers1060501942
pharmgkbrs1060501942
gwascentralrs1060501942
openSNPrs1060501942
23andMers1060501942
23andMe allrs1060501942
SNPshotrs1060501942
SNPdbers1060501942
MSV3drs1060501942
GWAS Ctlgrs1060501942
Max Magnitude0
ClinVar
Risk rs1060501942(-;-)
Alt rs1060501942(-;-)
Reference Rs1060501942(AACTT;AACTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131944990_131944994delCTTAA
CLNSRC
CLNACC RCV000457701.1,