Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs147277743
rs147277743
ATP13A2
0.050 GeneticVariation BEFREE The ATP13A2 A746T variant is rare in Han Chinese patients and controls and is not associated with PD susceptibility in this ethnic group. 26000924

2016
dbSNP: rs147277743
rs147277743
ATP13A2
0.050 GeneticVariation BEFREE We suggest that the ATP13A2 Ala746Thr variant is not a common risk factor for PD in the Chinese population in Hong Kong. 23522931

2013
dbSNP: rs147277743
rs147277743
ATP13A2
0.050 GeneticVariation BEFREE The clinical features and 99mTc-TRODAT-1 single photon emission computed tomography (SPECT) image of the patients carrying G1014S and A746T were similar to that of idiopathic PD. 21714071

2011
dbSNP: rs147277743
rs147277743
ATP13A2
0.050 GeneticVariation BEFREE These results suggest that ATP13A2 p.A746T variant is unlikely to play a role as a common risk factor or a pathogenic mutation for PD at least in Japanese. 20976737

2010
dbSNP: rs147277743
rs147277743
ATP13A2
0.050 GeneticVariation BEFREE We did not observe a significant association between Ala746Thr and Parkinson's disease in Han Chinese population, even after stratification by age at onset. 20227461

2010