Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6265
rs6265
0.030 GeneticVariation BEFREE The aim of our study was to (a) test for an association between the BDNF Val66Met polymorphism and childhood-onset melancholic depression and (b) to examine the interactive effects of stressful life events (SLE) and the Val66Met polymorphism on the risk of childhood-onset melancholic depression. 26462036

2015

dbSNP: rs6265
rs6265
0.030 GeneticVariation BEFREE Val66Met BDNF genotypes in melancholic depression: effects on brain structure and treatment outcome. 23165919

2013

dbSNP: rs6265
rs6265
0.030 GeneticVariation BEFREE However, BDNF rs7103411 and rs6265 similarly predicted worse treatment response over 6 wk in clinical subtypes of depression such as melancholic depression only (rs7103411: TT < CC, p = 0.003; rs6265: GG < AA, p = 0.001). 19236730

2010

dbSNP: rs759834365
rs759834365
0.020 GeneticVariation BEFREE The aim of our study was to (a) test for an association between the BDNF Val66Met polymorphism and childhood-onset melancholic depression and (b) to examine the interactive effects of stressful life events (SLE) and the Val66Met polymorphism on the risk of childhood-onset melancholic depression. 26462036

2015

dbSNP: rs759834365
rs759834365
0.020 GeneticVariation BEFREE Val66Met BDNF genotypes in melancholic depression: effects on brain structure and treatment outcome. 23165919

2013

dbSNP: rs6313
rs6313
0.010 GeneticVariation BEFREE About 62% of patients exhibiting the allelic combination of GG-GG-TT for rs6265, rs7430 and rs6313 of the BDNF, PPP3CC and HTR2A genes, respectively, and without melancholia showed a HAM-D decline under 17 compared to about 34% of the whole study sample. 25769916

2015

dbSNP: rs806371
rs806371
0.010 GeneticVariation BEFREE We observed a higher frequency of rs806371 G carriers in MD patients with both presence of melancholia (p = 0.018) and psychotic symptoms (p = 0.007) than in controls. 23407780

2013

dbSNP: rs58532686
rs58532686
0.010 GeneticVariation BEFREE An additional -/CT insertion/deletion (ins/del) polymorphism (rs58532686), however, was significantly associated with melancholic depression, with a better response in 12 patients carrying the deletion. 20588071

2010

dbSNP: rs7103411
rs7103411
0.010 GeneticVariation BEFREE However, BDNF rs7103411 and rs6265 similarly predicted worse treatment response over 6 wk in clinical subtypes of depression such as melancholic depression only (rs7103411: TT < CC, p = 0.003; rs6265: GG < AA, p = 0.001). 19236730

2010

dbSNP: rs25531
rs25531
0.010 GeneticVariation BEFREE Also, the more active 5-HTTLPR/5-HTT rs25531 haplotype L(A)L(A) conveyed a significant risk for melancholic depression (OR 2.0; 95%CI 1.3-3.1; P=0.001), again only in the female subsample of patients (OR 2.1; 95%CI 1.1-4.1; P=0.02). 18050262

2008

dbSNP: rs6295
rs6295
0.010 GeneticVariation BEFREE In order to further delineate the impact of 5-HT1A gene variation on pharmacoresponse in depression over 6 weeks of antidepressant treatment, the influence of the 5-HT1A-1019C/G (rs6295) polymorphism was investigated in 340 Caucasian patients with a Major Depressive Episode (DSM-IV) with particular attention to the subtype of depression (major depression and melancholic depression). 18387740

2008