Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis 		0.100 GeneticVariation GWASDB Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. 23603763

2013
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.100 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.100 GeneticVariation GWASDB Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. 22936693

2012
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.100 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233

2012
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.100 GeneticVariation GWASDB Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594

2012
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.100 GeneticVariation GWASDB Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. 22482804

2012
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.100 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661

2012
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0004096
Disease: Asthma
Asthma 		0.100 GeneticVariation GWASDB Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. 21150878

2011
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.100 GeneticVariation GWASDB Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. 21383967

2011
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.100 GeneticVariation GWASDB Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. 21383967

2011
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
Entrez Id: 116028
Gene Symbol: RMI2
RMI2
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.100 GeneticVariation GWASDB Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010