Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs174535
rs174535
MYRF ; TMEM258
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
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: 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: 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: 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: 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: rs174533
rs174533
MYRF ; TMEM258
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		A 0.700 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899

2017
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: rs174536
rs174536
MYRF ; TMEM258
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		A 0.700 GeneticVariation GWASCAT Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system. 29769521

2018
dbSNP: rs174536
rs174536
MYRF ; TMEM258
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		C 0.700 GeneticVariation GWASCAT Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality. 27798624

2016
dbSNP: rs174535
rs174535
MYRF ; TMEM258
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

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: rs174533
rs174533
MYRF ; TMEM258
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs174535
rs174535
MYRF ; TMEM258
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
dbSNP: rs174535
rs174535
MYRF ; TMEM258
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		T 0.700 GeneticVariation GWASCAT A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis. 30643255

2019
dbSNP: rs2071213
rs2071213
MYRF
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1 		A 0.700 GeneticVariation GWASCAT Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study. 29273593

2018
dbSNP: rs2071213
rs2071213
MYRF
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease 		A 0.700 GeneticVariation GWASCAT Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study. 29273593

2018
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		G 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516

2016
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		G 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286

2014
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		G 0.700 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: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		G 0.700 GeneticVariation GWASCAT GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12. 29471430

2018
dbSNP: rs174533
rs174533
MYRF ; TMEM258
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		G 0.700 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: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		G 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516

2016
dbSNP: rs174537
rs174537
MYRF ; TMEM258
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		G 0.700 GeneticVariation GWASCAT GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12. 29471430

2018