Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7793921
rs7793921
Entrez Id: 908;5723
Gene Symbol: CCT6A;PSPH
CCT6A;PSPH
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7793921
rs7793921
Entrez Id: 908;5723
Gene Symbol: CCT6A;PSPH
CCT6A;PSPH
CUI: C0201874
Disease:
Amino acids measurement 		G 0.700 GeneticVariation GWASCAT Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. 30659259 2019
dbSNP: rs7793921
rs7793921
Entrez Id: 908;5723
Gene Symbol: CCT6A;PSPH
CCT6A;PSPH
CUI: C0523888
Disease:
Serine measurement 		G 0.700 GeneticVariation GWASCAT Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. 30659259 2019
dbSNP: rs6593297
rs6593297
Entrez Id: 908;109616964
Gene Symbol: CCT6A;SNORA22B
CCT6A;SNORA22B
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs33922584
rs33922584
Entrez Id: 908
Gene Symbol: CCT6A
CCT6A
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma 		0.010 GeneticVariation BEFREE A low-frequency missense variant in chaperonin containing TCP1 subunit 6A gene (CCT6A) (rs33922584: adjusted hazard ratio [HR<sub>adjusted</sub>] = 1.75, p = 6.06 × 10<sup>-4</sup>) was significantly related to the survival of patients with NSCLC, which was further replicated by the TCGA samples (HR<sub>adjusted</sub> = 4.19, p = 0.015). 28104536 2017