Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2975226
rs2975226
0.020 GeneticVariation BEFREE In the dominant genetic model, the genotype AA+AT of rs2975226 in the Indian population (P<sub>z</sub> = 0, odds ratio [OR] = 3.245, 95% confidence interval [CI] = 1.806-5.831), TT of rs464049 (P<sub>z</sub> = 0.002, OR = 1.389, 95% CI = 1.129-1.708), and TT of rs3756450 (P<sub>z</sub> = 0.014, OR = 1.251, 95% CI = 1.047-1.495) might be risk factors for schizophrenia. 31440993

2020

dbSNP: rs27072
rs27072
0.020 GeneticVariation BEFREE All four polymorphisms (rs6347, intron8 5/6 VNTR, rs27072 and 3'UTR 9/10 VNTR) were genotyped in clinical cohorts, representing schizophrenia, bipolar disorder, depression, and controls. 21525861

2011

dbSNP: rs27072
rs27072
0.020 GeneticVariation BEFREE Six polymorphisms of the DAT1 gene (3 SNPs [rs6413429, rs2652511, and rs2975226] in the promoter region, one SNP [rs6347] in exon 9, and one SNP [rs27072]/one variable number tandem repeat [VNTR] in exon 15) were analyzed in 352 Chinese patients with schizophrenia and in 311 healthy controls. 19879111

2010

dbSNP: rs2975226
rs2975226
0.020 GeneticVariation BEFREE Six polymorphisms of the DAT1 gene (3 SNPs [rs6413429, rs2652511, and rs2975226] in the promoter region, one SNP [rs6347] in exon 9, and one SNP [rs27072]/one variable number tandem repeat [VNTR] in exon 15) were analyzed in 352 Chinese patients with schizophrenia and in 311 healthy controls. 19879111

2010

dbSNP: rs6347
rs6347
0.020 GeneticVariation BEFREE Thus the aim of the present study was to investigate the possible association between a new single nucleotide polymorphism (rs6347) located in exon 9 of the protein transporter (SLC6A3) and schizophrenia. 21049181

2010

dbSNP: rs6347
rs6347
0.020 GeneticVariation BEFREE Six polymorphisms of the DAT1 gene (3 SNPs [rs6413429, rs2652511, and rs2975226] in the promoter region, one SNP [rs6347] in exon 9, and one SNP [rs27072]/one variable number tandem repeat [VNTR] in exon 15) were analyzed in 352 Chinese patients with schizophrenia and in 311 healthy controls. 19879111

2010

dbSNP: rs464049
rs464049
0.010 GeneticVariation BEFREE In the dominant genetic model, the genotype AA+AT of rs2975226 in the Indian population (P<sub>z</sub> = 0, odds ratio [OR] = 3.245, 95% confidence interval [CI] = 1.806-5.831), TT of rs464049 (P<sub>z</sub> = 0.002, OR = 1.389, 95% CI = 1.129-1.708), and TT of rs3756450 (P<sub>z</sub> = 0.014, OR = 1.251, 95% CI = 1.047-1.495) might be risk factors for schizophrenia. 31440993

2020

dbSNP: rs2652511
rs2652511
0.010 GeneticVariation BEFREE Despite rs2652511 not being included, nor having any proxy SNP available in GWAS, the few candidate gene studies that analyzed it suggested an association with ADHD and schizophrenia. 24487615

2014

dbSNP: rs2455391
rs2455391
0.010 GeneticVariation BEFREE Two single nucleotide polymorphisms (SNPs) in the DAT1 gene (rs2975223 and rs2455391) were tested in 368 patients with schizophrenia and 420 healthy controls, of whom 293 patients underwent an assessment of psychotic symptoms through the positive and negative syndrome scale (PANSS). 22366190

2012

dbSNP: rs2270912
rs2270912
0.010 GeneticVariation BEFREE However, when the patient subgroup with verified familial history and the subgroup with early age of onset were re-analyzed, weak trend of association between 1398C>T SNP marker with schizophrenia was found in both cases. 15380858

2004