Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7191700
rs7191700
RMI2 ; LOC105371082
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
dbSNP: rs529866
rs529866
RMI2 ; LOC105371082
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		C 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233

2012
dbSNP: rs529866
rs529866
RMI2 ; LOC105371082
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017
dbSNP: rs4780355
rs4780355
SOCS1 ; RMI2 ; LOC105371082
CUI: C0033860
Disease: Psoriasis
Psoriasis 		T 0.800 GeneticVariation GWASCAT Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. 22482804

2012
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
CUI: C0033860
Disease: Psoriasis
Psoriasis 		C 0.800 GeneticVariation GWASCAT Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594

2012
dbSNP: rs1646019
rs1646019
RMI2 ; LOC105371082
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		G 0.800 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
dbSNP: rs1646019
rs1646019
RMI2 ; LOC105371082
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		A 0.800 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
dbSNP: rs12928822
rs12928822
RMI2 ; LOC105371082
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs80073729
rs80073729
RMI2 ; LOC105371082
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		G 0.700 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
dbSNP: rs80073729
rs80073729
RMI2 ; LOC105371082
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		A 0.700 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
dbSNP: rs77804393
rs77804393
RMI2 ; LOC105371082
CUI: C0013595
Disease: Eczema
Eczema 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs77061563
rs77061563
RMI2 ; LOC105371082
CUI: C0023343
Disease: Leprosy
Leprosy 		C 0.700 GeneticVariation GWASCAT Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy. 25642632

2015
dbSNP: rs7188861
rs7188861
RMI2 ; LOC105371082
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		A 0.700 GeneticVariation GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943

2015
dbSNP: rs6498184
rs6498184
RMI2 ; LOC105371082 ; LOC105371083
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.700 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013
dbSNP: rs529866
rs529866
RMI2 ; LOC105371082
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017
dbSNP: rs4781072
rs4781072
RMI2 ; LOC105371082
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs4780355
rs4780355
SOCS1 ; RMI2 ; LOC105371082
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.700 GeneticVariation GWASCAT Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. 22482804

2012
dbSNP: rs423674
rs423674
RMI2 ; LOC105371082
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		C 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs423674
rs423674
RMI2 ; LOC105371082
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
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