Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17309827
rs17309827
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0010346
Disease:
Crohn Disease
T 0.800 GeneticVariation GWASDB Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
dbSNP: rs17309827
rs17309827
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0010346
Disease:
Crohn Disease
T 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
dbSNP: rs17309827
rs17309827
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0010346
Disease:
Crohn Disease
0.800 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs12205405
rs12205405
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs58167401
rs58167401
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0427460
Disease:
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs58167401
rs58167401
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9503598
rs9503598
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs11759522
rs11759522
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0021704
Disease:
Intelligence
C 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs9503599
rs9503599
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs11759126
rs11759126
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
C 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs11759126
rs11759126
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0427460
Disease:
Red cell distribution width determination
C 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs4305775
rs4305775
Entrez Id: 63027;389362
Gene Symbol: SLC22A23;PSMG4
SLC22A23;PSMG4
CUI: C0008312
Disease:
Primary biliary cirrhosis
0.700 GeneticVariation GWASCAT A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. 28425483 2017
dbSNP: rs9503598
rs9503598
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694 2017
dbSNP: rs3734219
rs3734219
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0427460
Disease:
Red cell distribution width determination
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3734219
rs3734219
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs9378796
rs9378796
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0200665
Disease:
Platelet mean volume determination (procedure)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs13204048
rs13204048
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
A 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs13204048
rs13204048
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0010346
Disease:
Crohn Disease
A 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs9378357
rs9378357
Entrez Id: 63027;389362
Gene Symbol: SLC22A23;PSMG4
SLC22A23;PSMG4
CUI: C0162701
Disease:
Polysomnography
A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs4959235
rs4959235
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0280324
Disease:
Laryngeal Squamous Cell Carcinoma
0.010 GeneticVariation BEFREE To understand the association between SNPs in SLC22A23 and LSCC, selected genetic variations (rs4959235, rs6923667, rs9503518) were genotyped. 29703252 2018
dbSNP: rs9503518
rs9503518
Entrez Id: 63027;389362
Gene Symbol: SLC22A23;PSMG4
SLC22A23;PSMG4
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE 77.2% of patients were homozygote for genotype rs9503518-AA and they most frequently had histological grade 2 and 3 tumors. 29703252 2018
dbSNP: rs4959235
rs4959235
Entrez Id: 63027
Gene Symbol: SLC22A23
SLC22A23
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.010 GeneticVariation BEFREE Homozygocity for single-nucleotide polymorphisms rs4959235-TT and rs950318-GG was associated with IBD, whereby 6% of patients (18 of 311 cases) carried these genotypes, but they were not seen in healthy controls. 24740203 2014