CNTN5, contactin 5, 53942

N. diseases: 34; N. variants: 20
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1461677
rs1461677
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
dbSNP: rs67885470
rs67885470
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7927466
rs7927466
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0018099
Disease:
Gout 		A 0.700 GeneticVariation GWASCAT Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout. 31289104 2019
dbSNP: rs7927466
rs7927466
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0003868
Disease:
Arthritis, Gouty 		A 0.700 GeneticVariation GWASCAT Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout. 31289104 2019
dbSNP: rs10893002
rs10893002
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs10893002
rs10893002
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs1119257
rs1119257
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs17576589
rs17576589
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2614546
rs2614546
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs4316475
rs4316475
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs586533
rs586533
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C1269683
Disease:
Major Depressive Disorder 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs61475845
rs61475845
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C4722014
Disease:
Kynurenine Measurement 		A 0.700 GeneticVariation GWASCAT Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics. 29317604 2018
dbSNP: rs61475845
rs61475845
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C1269683
Disease:
Major Depressive Disorder 		A 0.700 GeneticVariation GWASCAT Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics. 29317604 2018
dbSNP: rs1690818
rs1690818
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0041696
Disease:
Unipolar Depression 		T 0.700 GeneticVariation GWASCAT Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. 27089181 2016
dbSNP: rs1690818
rs1690818
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C1269683
Disease:
Major Depressive Disorder 		T 0.700 GeneticVariation GWASCAT Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. 27089181 2016
dbSNP: rs1394461
rs1394461
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0205682
Disease:
Waist-Hip Ratio 		C 0.700 GeneticVariation GWASCAT New genetic loci link adipose and insulin biology to body fat distribution. 25673412 2015
dbSNP: rs11223581
rs11223581
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C2699541
Disease:
Cytokine Measurement 		G 0.700 GeneticVariation GWASCAT Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. 22610502 2012
dbSNP: rs1939697
rs1939697
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.700 GeneticVariation GWASDB Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. 23000144 2012
dbSNP: rs1939707
rs1939707
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.700 GeneticVariation GWASDB Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. 23000144 2012
dbSNP: rs1813443
rs1813443
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0010346
Disease:
Crohn Disease 		0.010 GeneticVariation BEFREE Based on our results, the rs1568885 and rs1813443 polymorphisms are associated with clinical and biochemical response to infliximab in Greek patients with Crohn's disease. 24707144 2014
dbSNP: rs6590474
rs6590474
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0003125
Disease:
Anorexia Nervosa 		0.010 GeneticVariation BEFREE The association analysis for MS-SNP haplotypes detected a statistically significant association (permutation P-value=0.00003) of the A-4-G-T haplotype that comprised four SNP/MS markers (rs6590474-D11S0268i-rs737582-rs7947224) on the 11q22 locus with AN. 19680270 2009
dbSNP: rs737582
rs737582
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0003125
Disease:
Anorexia Nervosa 		0.010 GeneticVariation BEFREE The association analysis for MS-SNP haplotypes detected a statistically significant association (permutation P-value=0.00003) of the A-4-G-T haplotype that comprised four SNP/MS markers (rs6590474-D11S0268i-rs737582-rs7947224) on the 11q22 locus with AN. 19680270 2009
dbSNP: rs7947224
rs7947224
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0003125
Disease:
Anorexia Nervosa 		0.010 GeneticVariation BEFREE The association analysis for MS-SNP haplotypes detected a statistically significant association (permutation P-value=0.00003) of the A-4-G-T haplotype that comprised four SNP/MS markers (rs6590474-D11S0268i-rs737582-rs7947224) on the 11q22 locus with AN. 19680270 2009
dbSNP: rs10501920
rs10501920
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0018802
Disease:
Congestive heart failure 		0.010 GeneticVariation BEFREE Also, rs10501920 in CNTN5 was associated with AF (p = 9.4 x 10(-6)) and HF (p = 1.2 x 10(-4)). 17903304 2007
dbSNP: rs10501920
rs10501920
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE Also, rs10501920 in CNTN5 was associated with AF (p = 9.4 x 10(-6)) and HF (p = 1.2 x 10(-4)). 17903304 2007