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rs1060501973

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501973(C;T)
Make rs1060501973(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132604850
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501973
dbSNP (old)rs1060501973
ClinGenrs1060501973
ebirs1060501973
HLIrs1060501973
Exacrs1060501973
Gnomadrs1060501973
Varsomers1060501973
Maprs1060501973
PheGenIrs1060501973
Biobankrs1060501973
1000 genomesrs1060501973
hgdprs1060501973
ensemblrs1060501973
gopubmedrs1060501973
geneviewrs1060501973
scholarrs1060501973
googlers1060501973
pharmgkbrs1060501973
gwascentralrs1060501973
openSNPrs1060501973
23andMers1060501973
23andMe allrs1060501973
SNPshotrs1060501973
SNPdbers1060501973
MSV3drs1060501973
GWAS Ctlgrs1060501973
Max Magnitude0
ClinVar
Risk rs1060501973(T;T)
Alt rs1060501973(T;T)
Reference Rs1060501973(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.131940542C>T
CLNSRC
CLNACC RCV000467015.1,