SLC24A3, solute carrier family 24 member 3, 57419

N. diseases: 34; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3790228
rs3790228
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0428883
Disease:
Diastolic blood pressure 		G 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs3828002
rs3828002
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4814884
rs4814884
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0037369
Disease:
Smoking 		T 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: rs6112527
rs6112527
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6035275
rs6035275
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0429028
Disease:
QT interval feature (observable entity) 		0.700 GeneticVariation GWASCAT Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group. 27958378 2018
dbSNP: rs6046226
rs6046226
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
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: rs4814864
rs4814864
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0149931
Disease:
Migraine Disorders 		C 0.700 GeneticVariation GWASCAT Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. 27322543 2016
dbSNP: rs6081569
rs6081569
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6081613
rs6081613
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0149931
Disease:
Migraine Disorders 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs6081541
rs6081541
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0033975
Disease:
Psychotic Disorders 		0.700 GeneticVariation GWASCAT Genome-wide association study of atypical psychosis. 24132900 2013
dbSNP: rs6081541
rs6081541
Entrez Id: 57419
Gene Symbol: SLC24A3
SLC24A3
CUI: C0029516
Disease:
Other and unspecified reactive psychosis 		0.700 GeneticVariation GWASCAT Genome-wide association study of atypical psychosis. 24132900 2013
dbSNP: rs3790171
rs3790171
Entrez Id: 57419;100130264
Gene Symbol: SLC24A3;LOC100130264
SLC24A3;LOC100130264
CUI: C0027819
Disease:
Neuroblastoma 		0.700 GeneticVariation GWASDB Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. 18463370 2008