Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1024611
rs1024611
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 GeneticVariation BEFREE <b>Results:</b>We found that the frequency of the CCL2 genotype of rs1024611</span> was significantly different between the PD and control groups (<i>p</i> = 0.021), while the C allele was associated with a significantly increased risk in the PD group (<i>p</i> = 0.004). 30761072

2019