CEP68, centrosomal protein 68, 23177

N. diseases: 13; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111524356
rs111524356
Entrez Id: 23177;107984063
Gene Symbol: CEP68;LOC107984063
CEP68;LOC107984063
CUI: C0202236
Disease:
Triglycerides measurement
0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs2249105
rs2249105
Entrez Id: 23177
Gene Symbol: CEP68
CEP68
CUI: C0202236
Disease:
Triglycerides measurement
0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs2540948
rs2540948
Entrez Id: 23177;107984063
Gene Symbol: CEP68;LOC107984063
CEP68;LOC107984063
CUI: C0202236
Disease:
Triglycerides measurement
T 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs2540948
rs2540948
Entrez Id: 23177;107984063
Gene Symbol: CEP68;LOC107984063
CEP68;LOC107984063
CUI: C0202236
Disease:
Triglycerides measurement
C 0.700 GeneticVariation GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943 2015