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rs1060501970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501970(A;C)
Make rs1060501970(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132579860
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501970
dbSNP (old)rs1060501970
ClinGenrs1060501970
ebirs1060501970
HLIrs1060501970
Exacrs1060501970
Gnomadrs1060501970
Varsomers1060501970
LitVarrs1060501970
Maprs1060501970
PheGenIrs1060501970
Biobankrs1060501970
1000 genomesrs1060501970
hgdprs1060501970
ensemblrs1060501970
gopubmedrs1060501970
geneviewrs1060501970
scholarrs1060501970
googlers1060501970
pharmgkbrs1060501970
gwascentralrs1060501970
openSNPrs1060501970
23andMers1060501970
23andMe allrs1060501970
SNPshotrs1060501970
SNPdbers1060501970
MSV3drs1060501970
GWAS Ctlgrs1060501970
Max Magnitude0
ClinVar
Risk rs1060501970(C;C)
Alt rs1060501970(C;C)
Reference Rs1060501970(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131915552A>C
CLNSRC
CLNACC RCV000458636.1,