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rs1060501936

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501936(C;T)
Make rs1060501936(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132603989
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501936
dbSNP (old)rs1060501936
ClinGenrs1060501936
ebirs1060501936
HLIrs1060501936
Exacrs1060501936
Gnomadrs1060501936
Varsomers1060501936
Maprs1060501936
PheGenIrs1060501936
Biobankrs1060501936
1000 genomesrs1060501936
hgdprs1060501936
ensemblrs1060501936
gopubmedrs1060501936
geneviewrs1060501936
scholarrs1060501936
googlers1060501936
pharmgkbrs1060501936
gwascentralrs1060501936
openSNPrs1060501936
23andMers1060501936
23andMe allrs1060501936
SNPshotrs1060501936
SNPdbers1060501936
MSV3drs1060501936
GWAS Ctlgrs1060501936
Max Magnitude0
ClinVar
Risk rs1060501936(T;T)
Alt rs1060501936(T;T)
Reference Rs1060501936(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131939681C>T
CLNSRC
CLNACC RCV000458297.1,