Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75854315
rs75854315
Entrez Id: 23381
Gene Symbol: SMG5
SMG5
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs75854315
rs75854315
Entrez Id: 23381
Gene Symbol: SMG5
SMG5
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2241106
rs2241106
Entrez Id: 23381;79957
Gene Symbol: SMG5;PAQR6
SMG5;PAQR6
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs6684514
rs6684514
Entrez Id: 23381;84283
Gene Symbol: SMG5;TMEM79
SMG5;TMEM79
CUI: C0518015
Disease:
Hemoglobin measurement 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of hematological and biochemical traits in a Japanese population. 20139978 2010
dbSNP: rs6684514
rs6684514
Entrez Id: 23381;84283
Gene Symbol: SMG5;TMEM79
SMG5;TMEM79
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of hematological and biochemical traits in a Japanese population. 20139978 2010
dbSNP: rs6684514
rs6684514
Entrez Id: 23381;84283
Gene Symbol: SMG5;TMEM79
SMG5;TMEM79
CUI: C0011615
Disease:
Dermatitis, Atopic 		0.010 GeneticVariation BEFREE Meta-analysis of 4,245 AD cases and 10,558 population-matched control subjects showed that a missense SNP, rs6684514, [corrected] in the human MATT gene has a small but significant association with AD. 24084074 2013
dbSNP: rs6684514
rs6684514
Entrez Id: 23381;84283
Gene Symbol: SMG5;TMEM79
SMG5;TMEM79
CUI: C0013595
Disease:
Eczema 		0.010 GeneticVariation BEFREE Meta-analysis of 4,245 AD cases and 10,558 population-matched control subjects showed that a missense SNP, rs6684514, [corrected] in the human MATT gene has a small but significant association with AD. 24084074 2013