Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs117322666
rs117322666
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
CUI: C1278049
Disease:
Serum gamma-glutamyl transferase measurement 		0.700 GeneticVariation GWASCAT Biomarker and Genomic Risk Factors for Liver Function Test Abnormality in Hazardous Drinkers. 30589442 2019
dbSNP: rs10964221
rs10964221
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
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: rs1887489
rs1887489
Entrez Id: 25769;105375988
Gene Symbol: SLC24A2;LOC105375988
SLC24A2;LOC105375988
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs1887489
rs1887489
Entrez Id: 25769;105375988
Gene Symbol: SLC24A2;LOC105375988
SLC24A2;LOC105375988
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs2383101
rs2383101
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
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: rs4977397
rs4977397
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.700 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015 2018
dbSNP: rs6475417
rs6475417
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
CUI: C0038663
Disease:
Suicide attempt 		G 0.700 GeneticVariation GWASCAT Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study. 30116032 2018
dbSNP: rs6475417
rs6475417
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
CUI: C0525045
Disease:
Mood Disorders 		G 0.700 GeneticVariation GWASCAT Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study. 30116032 2018
dbSNP: rs7870850
rs7870850
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs7870850
rs7870850
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs10738554
rs10738554
Entrez Id: 25769
Gene Symbol: SLC24A2
SLC24A2
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE The most significant result among all univariate and multivariate tests performed in this study was the heterogeneity of correlation between PAI-1 and mean arterial pressure at rs10738554, near SLC24A2, a gene previously associated with high blood pressure in African Americans. 28408189 2017