Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2234253
rs2234253
Entrez Id: 54209;105375056
Gene Symbol: TREM2;LOC105375056
TREM2;LOC105375056
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE No variant for either rs75932628 or rs2234253 was found in both PD and control cohorts. 26704436 2016