Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation BEFREE To determine whether dopaminergic (rs1076560 DRD2 G > T and rs4680 catechole-o-methyltranspherase (COMT) Val158Met) or brain derived neurotrophic factor (rs6265 BDNF Val66Met) genetic polymorphisms are associated with gait function and medication responsiveness in Parkinson's disease. 29249680

2018
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation BEFREE We estimated and compared the haplotype frequencies between C270T and G196A markers in PD and controls that was positive (p = 0.0019). 15120095

2004
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation BEFREE Our meta-analysis implicates Val66Met BDNF polymorphism may be associated with Parkinson's disease cognitive impairment, further well-designed studies with larger populations are required to validate these results owing to the limited research. 31104169

2019