Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2903692
rs2903692
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.840 GeneticVariation BEFREE rs2903692 conferred a protective effect on patients with T1D, MS and RA. 19221398 2010
dbSNP: rs2903692
rs2903692
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.840 GeneticVariation BEFREE Independent genome-wide association studies highlighted the function of CLEC16A/KIAA0350 polymorphisms modifying the risk to either multiple sclerosis (rs6498169) or type 1 diabetes (rs2903692). 19337309 2009
dbSNP: rs2903692
rs2903692
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.840 GeneticVariation BEFREE Furthermore, a joint analysis, with the INS and CTLA4 SNPs, revealed that CTLA4 rs3087243, ERBB3 rs2292399, and CLEC16A rs2903692, but not INS rs689, were significant risk factors for the cooccurrence of AITD in Japanese T1D. 18940880 2009
dbSNP: rs2903692
rs2903692
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
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: rs2903692
rs2903692
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.840 GeneticVariation BEFREE 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: rs2903692
rs2903692
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		G 0.840 GeneticVariation GWASDB 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
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0024141
Disease:
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: rs12599402
rs12599402
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		A 0.810 GeneticVariation GWASDB 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: rs12599402
rs12599402
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		0.810 GeneticVariation BEFREE The association between SNP rs12599402 and SLE reached the genome-wide significance level (p<5 × 10⁻⁸). 20805369 2011
dbSNP: rs12924729
rs12924729
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
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: rs12927355
rs12927355
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
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: rs7203459
rs7203459
Entrez Id: 23274;105371081
Gene Symbol: CLEC16A;LOC105371081
CLEC16A;LOC105371081
CUI: C1527304
Disease:
Allergic Reaction 		C 0.800 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs7203459
rs7203459
Entrez Id: 23274;105371081
Gene Symbol: CLEC16A;LOC105371081
CLEC16A;LOC105371081
CUI: C1527304
Disease:
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: rs12708715
rs12708715
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
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
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.800 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012
dbSNP: rs12708715
rs12708715
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
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
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		C 0.800 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012
dbSNP: rs12924729
rs12924729
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.800 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012
dbSNP: rs12708716
rs12708716
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		G 0.800 GeneticVariation GWASCAT Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. 21829393 2011
dbSNP: rs12924729
rs12924729
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635 2011
dbSNP: rs12924729
rs12924729
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0008312
Disease:
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
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.800 GeneticVariation GWASDB A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. 21980299 2011
dbSNP: rs7200786
rs7200786
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs7200786
rs7200786
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs11865121
rs11865121
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0026769
Disease:
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