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rs1060501954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs1060501954(-;-)
Make rs1060501954(-;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132589638
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501954
dbSNP (old)rs1060501954
ClinGenrs1060501954
ebirs1060501954
HLIrs1060501954
Exacrs1060501954
Gnomadrs1060501954
Varsomers1060501954
Maprs1060501954
PheGenIrs1060501954
Biobankrs1060501954
1000 genomesrs1060501954
hgdprs1060501954
ensemblrs1060501954
gopubmedrs1060501954
geneviewrs1060501954
scholarrs1060501954
googlers1060501954
pharmgkbrs1060501954
gwascentralrs1060501954
openSNPrs1060501954
23andMers1060501954
23andMe allrs1060501954
SNPshotrs1060501954
SNPdbers1060501954
MSV3drs1060501954
GWAS Ctlgrs1060501954
Max Magnitude0
ClinVar
Risk rs1060501954(-;-)
Alt rs1060501954(-;-)
Reference Rs1060501954(TT;TT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131925330_131925331delTT
CLNSRC
CLNACC RCV000457032.1,