rs3851179, None

N. diseases: 8
Source: ALL
Disease Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.020 GeneticVariation BEFREE Our finding suggests that PICALM rs3851179 could contribute to cognitive impairment in older patients with PD. 26889634 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.020 GeneticVariation BEFREE The two other SNPs, rs6656401 from CR1, and rs3851179 from PICALM region were not associated with PD (p>0.05). 21912625 2011