Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801133
rs1801133
0.010 GeneticVariation BEFREE Nevertheless, the frequency of the <i>G</i> allele of rs1801133 of <i>MTHFR</i> was higher in the RDD group and the frequency of the <i>C</i> allele of rs6264 of <i>BDNF</i> was higher in the MDD group. 27994504

2016

dbSNP: rs5443
rs5443
0.010 GeneticVariation BEFREE This study was conducted to explore the possibility of association between the single-nucleotide polymorphisms rs6264 of <i>BDNF</i>, rs5443 of <i>GNB3</i>, and rs1801133 of <i>MTHFR</i>; the <i>In/Del</i> polymorphism of <i>ACE</i>; and the <i>ε2</i> allele of <i>APOE</i> and major depressive disorder (MDD) and recurrent depressive disorder (RDD) in an East Slavic population. 27994504

2016

dbSNP: rs6264
rs6264
DDC
0.010 GeneticVariation BEFREE Nevertheless, the frequency of the <i>G</i> allele of rs1801133 of <i>MTHFR</i> was higher in the RDD group and the frequency of the <i>C</i> allele of rs6264 of <i>BDNF</i> was higher in the MDD group. 27994504

2016

dbSNP: rs225014
rs225014
0.010 GeneticVariation BEFREE The specific variant of the DIO2 gene, namely the CC genotype of the Thr92Ala polymorphism, was more frequently found in healthy subjects than in patients with depression, what suggests that it could potentially serve as a marker of a lower risk for recurrent depressive disorder. 26098717

2015

dbSNP: rs2010963
rs2010963
0.010 GeneticVariation BEFREE The aim of the study was to analyze the association between VEGFA gene polymorphisms (+405G/C; rs2010963, +936C/T; rs 3025039), VEGFA gene expression, and its serum protein levels in rDD in the Caucasian population. 23673188

2013

dbSNP: rs56149945
rs56149945
0.010 GeneticVariation BEFREE The presence of C allele, CC, and GC genotype of BclI polymorphism, G allele and GA genotype for N363S and ER22/23EK variants respectively were associated with increased rDD risk. 23073785

2013

dbSNP: rs4753426
rs4753426
0.010 GeneticVariation BEFREE We found an increased risk for rDD in patients with the C allele and a decreased risk in patients with the T allele (rs4753426). 21353709

2011

dbSNP: rs1141718
rs1141718
0.010 GeneticVariation BEFREE Analysis of two polymorphisms of the manganese superoxide dismutase gene (Ile-58Thr and Ala-9Val) in patients with recurrent depressive disorder. 20478627

2010

dbSNP: rs953038635
rs953038635
0.010 GeneticVariation BEFREE Analysis of two polymorphisms of the manganese superoxide dismutase gene (Ile-58Thr and Ala-9Val) in patients with recurrent depressive disorder. 20478627

2010