Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1136141
rs1136141
Entrez Id: 3312;101929289
Gene Symbol: HSPA8;LOC101929289
HSPA8;LOC101929289
CUI: C0338614
Disease:
Psychotic episodes
0.010 GeneticVariation BEFREE Our results showed that FEP patients presented a polymorphism differentiation related to the HSPA8 gene (rs1136141), and a higher frequency of T carriers compared to healthy controls was observed. 24548631 2014
dbSNP: rs2236659
rs2236659
Entrez Id: 3312;101929289
Gene Symbol: HSPA8;LOC101929289
HSPA8;LOC101929289
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE These findings suggest that genetic variants in HSPA8 gene (especially promoter SNP rs2236659) contribute to the CHD susceptibility by affecting its expression level. 20300519 2010
dbSNP: rs1366901063
rs1366901063
Entrez Id: 3312;85389;85390;101929289
Gene Symbol: HSPA8;SNORD14C;SNORD14D;LOC101929289
HSPA8;SNORD14C;SNORD14D;LOC101929289
CUI: C4511452
Disease:
Sporadic Parkinson disease
0.010 GeneticVariation BEFREE We propose that aberrant interactions of UCH-L1 variants with CMA machinery, at least partly, underlie the pathogenesis of I93M UCH-L1-associated PD, and possibly of sporadic PD. 18635949 2008
dbSNP: rs1366901063
rs1366901063
Entrez Id: 3312;85389;85390;101929289
Gene Symbol: HSPA8;SNORD14C;SNORD14D;LOC101929289
HSPA8;SNORD14C;SNORD14D;LOC101929289
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Our findings may provide novel insights into the molecular links between alpha-synuclein and UCH-L1 and suggest that aberrant interaction of mutant UCH-L1 with CMA machinery, at least partly, underlies the pathogenesis of PD associated with I93M UCH-L1. 18550537 2008
dbSNP: rs2236659
rs2236659
Entrez Id: 3312;101929289
Gene Symbol: HSPA8;LOC101929289
HSPA8;LOC101929289
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4802
rs4802
Entrez Id: 3312;85391
Gene Symbol: HSPA8;SNORD14E
HSPA8;SNORD14E
CUI: C0019693
Disease:
HIV Infections
0.700 GeneticVariation GWASCAT Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 26148204 2015
dbSNP: rs4802
rs4802
Entrez Id: 3312;85391
Gene Symbol: HSPA8;SNORD14E
HSPA8;SNORD14E
CUI: C0373595
Disease:
Creatinine clearance measurement
0.700 GeneticVariation GWASCAT Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 26148204 2015
dbSNP: rs4936770
rs4936770
Entrez Id: 3312;85391
Gene Symbol: HSPA8;SNORD14E
HSPA8;SNORD14E
CUI: C0373595
Disease:
Creatinine clearance measurement
0.700 GeneticVariation GWASCAT Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 26148204 2015
dbSNP: rs4936770
rs4936770
Entrez Id: 3312;85391
Gene Symbol: HSPA8;SNORD14E
HSPA8;SNORD14E
CUI: C0019693
Disease:
HIV Infections
0.700 GeneticVariation GWASCAT Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 26148204 2015