Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074175
rs120074175
TPH2
0.010 GeneticVariation BEFREE A variant of TPH2 that encodes the R441H substitution (TPH2-R441H) was identified in individuals with severe depression. 31071306

2019
dbSNP: rs7041
rs7041
GC
0.010 GeneticVariation BEFREE This study showed that an HP/LF diet interacts with the rs7041 polymorphism, with T allele carriers having a greater prevalence of moderate and severe depression. 30184533

2018