rs17309827
|
SLC22A23
|
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 |
rs17309827
|
SLC22A23
|
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 |
rs17309827
|
SLC22A23
|
Crohn Disease
|
|
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
rs12205405
|
SLC22A23
|
Finding of Mean Corpuscular Hemoglobin
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs58167401
|
SLC22A23
|
Red cell distribution width determination
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs58167401
|
SLC22A23
|
RDW - Red blood cell distribution width result
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs9503598
|
SLC22A23
|
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 |
rs11759522
|
SLC22A23
|
Intelligence
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
|
29844566 |
2018 |
rs9503599
|
SLC22A23
|
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 |
rs11759126
|
SLC22A23
|
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 |
rs11759126
|
SLC22A23
|
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 |
rs4305775
|
SLC22A23;PSMG4
|
Primary biliary cirrhosis
|
|
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis.
|
28425483 |
2017 |
rs9503598
|
SLC22A23
|
Intelligence
|
|
0.700 |
GeneticVariation |
GWASCAT |
Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets.
|
29186694 |
2017 |
rs3734219
|
SLC22A23
|
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 |
rs3734219
|
SLC22A23
|
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 |
rs9378796
|
SLC22A23
|
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 |
rs13204048
|
SLC22A23
|
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 |
rs13204048
|
SLC22A23
|
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 |
rs9378357
|
SLC22A23;PSMG4
|
Polysomnography
|
A |
0.700 |
GeneticVariation |
GWASDB |
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
|
23251661 |
2012 |
rs4959235
|
SLC22A23
|
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 |
rs9503518
|
SLC22A23;PSMG4
|
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 |
rs4959235
|
SLC22A23
|
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 |