Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582

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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASCAT GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12. 29471430

2018
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516

2016
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286

2014
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: 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: rs174528
rs174528
MYRF ; TMEM258
CUI: C2316832
Disease: Arachidonic acid measurement
Arachidonic acid measurement 		T 0.700 GeneticVariation GWASCAT A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. 26584805

2015
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: rs174529
rs174529
MYRF ; TMEM258
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		T 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		T 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		T 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		T 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
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: rs174529
rs174529
MYRF ; TMEM258
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		C 0.700 GeneticVariation GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943

2015
dbSNP: rs174529
rs174529
MYRF ; TMEM258
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		T 0.700 GeneticVariation GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943

2015
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: 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: rs174533
rs174533
MYRF ; TMEM258
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019
dbSNP: rs174533
rs174533
MYRF ; TMEM258
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019