Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11940117
rs11940117
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0042900
Disease:
Vitiligo 		0.010 GeneticVariation BEFREE The aim of this study was to evaluate the potential influence of 10 single-nucleotide polymorphisms (SNPs) at 18q21.31 (rs10503019), 4p16.1 (rs11940117), 3q28 (rs1464510), 14q12 (rs2273844), 12q13.2 (rs2456973), 16q12.2 (rs3213758), 10q25.3 (rs4353229), 3q13.33 (rs59374417), and 10p15.1 (rs706779 and rs7090530) on vitiligo with immune-related diseases in the Chinese Han population. 25952005 2015
dbSNP: rs11940117
rs11940117
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C1847835
Disease:
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		0.010 GeneticVariation BEFREE The aim of this study was to evaluate the potential influence of 10 single-nucleotide polymorphisms (SNPs) at 18q21.31 (rs10503019), 4p16.1 (rs11940117), 3q28 (rs1464510), 14q12 (rs2273844), 12q13.2 (rs2456973), 16q12.2 (rs3213758), 10q25.3 (rs4353229), 3q13.33 (rs59374417), and 10p15.1 (rs706779 and rs7090530) on vitiligo with immune-related diseases in the Chinese Han population. 25952005 2015
dbSNP: rs12504795
rs12504795
Entrez Id: 116449;105374482
Gene Symbol: CLNK;LOC105374482
CLNK;LOC105374482
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.800 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs13142500
rs13142500
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0003873
Disease:
Rheumatoid Arthritis 		T 0.800 GeneticVariation GWASCAT Genetic influences on susceptibility to rheumatoid arthritis in African-Americans. 30423114 2019
dbSNP: rs13142500
rs13142500
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0003873
Disease:
Rheumatoid Arthritis 		C 0.800 GeneticVariation GWASCAT Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342 2014
dbSNP: rs16872571
rs16872571
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0042900
Disease:
Vitiligo 		C 0.800 GeneticVariation GWASCAT Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. 22561518 2012
dbSNP: rs11721691
rs11721691
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs16872571
rs16872571
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0154778
Disease:
Myopia, Degenerative 		0.700 GeneticVariation GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088 2012
dbSNP: rs4293777
rs4293777
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0008313
Disease:
Cholangitis, Sclerosing 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease. 27992413 2017
dbSNP: rs4293777
rs4293777
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56817615
rs56817615
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0004364
Disease:
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56817615
rs56817615
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56817615
rs56817615
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56817615
rs56817615
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7675668
rs7675668
Entrez Id: 116449;105374482
Gene Symbol: CLNK;LOC105374482
CLNK;LOC105374482
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		C 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs12504795
rs12504795
Entrez Id: 116449;105374482
Gene Symbol: CLNK;LOC105374482
CLNK;LOC105374482
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASDB Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. 19503597 2009
dbSNP: rs13142500
rs13142500
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0003873
Disease:
Rheumatoid Arthritis 		C 0.800 GeneticVariation GWASDB Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342 2014
dbSNP: rs16872571
rs16872571
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0042900
Disease:
Vitiligo 		C 0.800 GeneticVariation GWASDB Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. 22561518 2012
dbSNP: rs10001632
rs10001632
Entrez Id: 116449;105374482
Gene Symbol: CLNK;LOC105374482
CLNK;LOC105374482
CUI: C0018099
Disease:
Gout 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013
dbSNP: rs10001632
rs10001632
Entrez Id: 116449;105374482
Gene Symbol: CLNK;LOC105374482
CLNK;LOC105374482
CUI: C0003868
Disease:
Arthritis, Gouty 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013
dbSNP: rs10030521
rs10030521
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASDB Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. 19503597 2009
dbSNP: rs10030521
rs10030521
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0018099
Disease:
Gout 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013
dbSNP: rs10030521
rs10030521
Entrez Id: 116449
Gene Symbol: CLNK
CLNK
CUI: C0003868
Disease:
Arthritis, Gouty 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013
dbSNP: rs10033825
rs10033825
Entrez Id: 116449;105374482
Gene Symbol: CLNK;LOC105374482
CLNK;LOC105374482
CUI: C0018099
Disease:
Gout 		0.700 GeneticVariation GWASDB Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. 20884846 2010
dbSNP: rs10033825
rs10033825
Entrez Id: 116449;105374482
Gene Symbol: CLNK;LOC105374482
CLNK;LOC105374482
CUI: C0018099
Disease:
Gout 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013