Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12720208
rs12720208
FGF20
0.060 GeneticVariation BEFREE This meta-analysis indicates that rs12720208 C/T variant might be associated with PD susceptibility in Caucasians. 28191856

2017
dbSNP: rs12720208
rs12720208
FGF20
0.060 GeneticVariation BEFREE Our results suggest that there is no sufficient evidence to support the association between rs12720208 polymorphism and PD risk. 27023076

2016
dbSNP: rs12720208
rs12720208
FGF20
0.060 GeneticVariation BEFREE Our results suggest that the rs12720208 polymorphism may be a risk factor for PD in Iranian population. 26070653

2015
dbSNP: rs12720208
rs12720208
FGF20
0.060 GeneticVariation BEFREE For rs12720208 (C/T) polymorphism, there was no significant difference in genotype distribution and gender and age-related differences between PD and control group. 22342445

2012
dbSNP: rs12720208
rs12720208
FGF20
0.060 GeneticVariation BEFREE In conclusion, our work did not confirm the association between rs12720208 and PD, or an effect of miR-433 variants on this disease. 20471450

2010
dbSNP: rs12720208
rs12720208
FGF20
0.060 GeneticVariation BEFREE We found no evidence of association between FGF20 variability and PD risk, and no relationship between the rs12720208 genotype, FGF20 and alpha-synuclein protein levels. 19133659

2009