Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1900599
rs1900599
Entrez Id: 145581
Gene Symbol: LRFN5
LRFN5
CUI: C1269683
Disease:
Major Depressive Disorder
A 0.700 GeneticVariation GWASCAT Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. 29662059 2018