Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584

2019
dbSNP: rs509360
rs509360
MYRF ; TMEM258
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs174530
rs174530
MYRF ; TMEM258
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs174535
rs174535
MYRF ; TMEM258
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		T 0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738

2019
dbSNP: rs174535
rs174535
MYRF ; TMEM258
CUI: C0004096
Disease: Asthma
Asthma 		T 0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738

2019
dbSNP: rs174533
rs174533
MYRF ; TMEM258
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASCAT Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. 31393916

2019
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		T 0.800 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531

2018
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		T 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531

2018
dbSNP: rs7943728
rs7943728
MYRF ; TMEM258
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs7943728
rs7943728
MYRF ; TMEM258
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174533
rs174533
MYRF ; TMEM258
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174533
rs174533
MYRF ; TMEM258
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174530
rs174530
MYRF ; TMEM258
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174530
rs174530
MYRF ; TMEM258
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174528
rs174528
MYRF ; TMEM258
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs174528
rs174528
MYRF ; TMEM258
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs11320420
rs11320420
MYRF ; TMEM258
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs11320420
rs11320420
MYRF ; TMEM258
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs2956395
rs2956395
MYRF ; MYRF-AS1
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 30 loci associated with bipolar disorder. 31043756

2019
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935

2017
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935

2017
dbSNP: rs61896141
rs61896141
MYRF ; TMEM258
CUI: C0018498
Disease: Hair Color
Hair Color 		C 0.700 GeneticVariation GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825

2018