Disease: Parkinsonian Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1224426272
rs1224426272
Entrez Id: 11113
Gene Symbol: CIT
CIT
CUI: C0242422
Disease:
Parkinsonian Disorders 		0.010 GeneticVariation BEFREE Serotonergic pathology and disease burden in the premotor and motor phase of A53T α-synuclein parkinsonism: a cross-sectional study. 31229470 2019