SDK1, sidekick cell adhesion molecule 1, 221935

N. diseases: 18; N. variants: 41
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10242223
rs10242223
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0017168
Disease:
Gastroesophageal reflux disease 		A 0.700 GeneticVariation GWASCAT Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. 31527586 2019
dbSNP: rs1108879
rs1108879
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs117749317
rs117749317
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0523953
Disease:
Cardiac troponin T measurement 		A 0.700 GeneticVariation GWASCAT Cardiac Troponin T and Troponin I in the General Population. 31014085 2019
dbSNP: rs13237637
rs13237637
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0037369
Disease:
Smoking 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs6462203
rs6462203
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0003469
Disease:
Anxiety Disorders 		C 0.700 GeneticVariation GWASCAT Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. 31116379 2019
dbSNP: rs10085617
rs10085617
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C3160814
Disease:
Cannabis use 		A 0.700 GeneticVariation GWASCAT GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia. 30150663 2018
dbSNP: rs1019914
rs1019914
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10951155
rs10951155
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs17133347
rs17133347
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs4257931
rs4257931
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0596887
Disease:
mathematical ability 		G 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: rs4336505
rs4336505
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs4719944
rs4719944
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs959894
rs959894
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs34912216
rs34912216
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0026603
Disease:
Motion Sickness 		G 0.700 GeneticVariation GWASCAT Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. 25628336 2015
dbSNP: rs4343996
rs4343996
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0026603
Disease:
Motion Sickness 		G 0.700 GeneticVariation GWASCAT Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. 25628336 2015
dbSNP: rs17134117
rs17134117
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0004352
Disease:
Autistic Disorder 		0.700 GeneticVariation GWASDB A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. 22935194 2013
dbSNP: rs10234405
rs10234405
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10237319
rs10237319
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10237488
rs10237488
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10237838
rs10237838
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10265937
rs10265937
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10266101
rs10266101
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10278187
rs10278187
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs10485860
rs10485860
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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: rs12155314
rs12155314
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
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