Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2903692
rs2903692
CLEC16A
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		G 0.840 GeneticVariation GWASCAT Three common non-coding variants of the gene (rs2903692, rs725613 and rs17673553) in strong linkage disequilibrium reached genome-wide significance for association with T1D. 17632545

2007
dbSNP: rs12599402
rs12599402
CLEC16A
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		A 0.810 GeneticVariation GWASCAT Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568

2013
dbSNP: rs11865121
rs11865121
CLEC16A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.800 GeneticVariation GWASCAT Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs12708715
rs12708715
CLEC16A
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: rs12708715
rs12708715
CLEC16A
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: rs12708715
rs12708715
CLEC16A
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		C 0.800 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
dbSNP: rs12708716
rs12708716
CLEC16A
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		G 0.800 GeneticVariation GWASCAT Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. 21829393

2011
dbSNP: rs12708716
rs12708716
CLEC16A
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 GeneticVariation GWASCAT Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. 19430480

2009
dbSNP: rs12708716
rs12708716
CLEC16A
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		G 0.800 GeneticVariation GWASCAT Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. 18978792

2008
dbSNP: rs12708716
rs12708716
CLEC16A
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		A 0.800 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007
dbSNP: rs12708716
rs12708716
CLEC16A
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		A 0.800 GeneticVariation GWASCAT Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. 17554260

2007
dbSNP: rs12924729
rs12924729
CLEC16A
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		G 0.800 GeneticVariation GWASCAT International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. 26394269

2015
dbSNP: rs12924729
rs12924729
CLEC16A
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635

2011
dbSNP: rs12927355
rs12927355
CLEC16A
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		C 0.800 GeneticVariation GWASCAT Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. 25751624

2015
dbSNP: rs7200786
rs7200786
CLEC16A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs7203459
rs7203459
CLEC16A ; LOC105371081
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		C 0.800 GeneticVariation GWASCAT A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569

2013
dbSNP: rs62026376
rs62026376
CLEC16A ; LOC105371081
CUI: C0004096
Disease: Asthma
Asthma 		C 0.710 GeneticVariation GWASCAT The rs62026376:C allele associated with increased asthma with hay fever risk has been found to be associated also with decreased expression of the nearby DEXI gene in monocytes. 24388013

2014
dbSNP: rs62026376
rs62026376
CLEC16A ; LOC105371081
CUI: C0018621
Disease: Hay fever
Hay fever 		C 0.710 GeneticVariation GWASCAT The rs62026376:C allele associated with increased asthma with hay fever risk has been found to be associated also with decreased expression of the nearby DEXI gene in monocytes. 24388013

2014
dbSNP: rs11644510
rs11644510
CLEC16A
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		C 0.700 GeneticVariation GWASCAT Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. 30013184

2018
dbSNP: rs11644510
rs11644510
CLEC16A
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		C 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406

2017
dbSNP: rs11644510
rs11644510
CLEC16A
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs11645657
rs11645657
CLEC16A ; LOC105371081
CUI: C0004096
Disease: Asthma
Asthma 		0.700 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011

2018
dbSNP: rs11645657
rs11645657
CLEC16A ; LOC105371081
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011

2018
dbSNP: rs12924112
rs12924112
CLEC16A
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		0.700 GeneticVariation GWASCAT Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis. 29904099

2019
dbSNP: rs12924729
rs12924729
CLEC16A
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635

2011