TST, thiosulfate sulfurtransferase, 7263

N. diseases: 91; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5756482
rs5756482
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs5756487
rs5756487
Entrez Id: 4357;7263
Gene Symbol: MPST;TST
MPST;TST
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: rs5756487
rs5756487
Entrez Id: 4357;7263
Gene Symbol: MPST;TST
MPST;TST
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs130598
rs130598
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs130599
rs130599
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs130607
rs130607
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs5750366
rs5750366
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs5750370
rs5750370
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs5756477
rs5756477
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs5756477
rs5756477
Entrez Id: 7263
Gene Symbol: TST
TST
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
dbSNP: rs774437307
rs774437307
Entrez Id: 4357;7263
Gene Symbol: MPST;TST
MPST;TST
CUI: C1867326
Disease:
RETINAL CONE DYSTROPHY 1 		0.010 GeneticVariation BEFREE We report a mutation (Y99C) in guanylate cyclase activator 1A (GUCA1A), the gene for guanylate cyclase activating protein (GCAP1), in a family with autosomal dominant cone dystrophy. 9425234 1998
dbSNP: rs775639597
rs775639597
Entrez Id: 4357;7263
Gene Symbol: MPST;TST
MPST;TST
CUI: C1405854
Disease:
Retinitis punctata albescens (disorder) 		0.010 GeneticVariation BEFREE Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene. 8554077 1996