Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519291
rs1057519291
ATP13A2
A 0.800 CausalMutation CLINVAR

dbSNP: rs1057519291
rs1057519291
ATP13A2
0.800 GeneticVariation UNIPROT

dbSNP: rs758014228
rs758014228
ATP13A2
C 0.700 GeneticVariation CLINVAR Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9). 21696388

2012
dbSNP: rs758014228
rs758014228
ATP13A2
C 0.700 GeneticVariation CLINVAR Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. 16964263

2006
dbSNP: rs1057519289
rs1057519289
ATP13A2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519290
rs1057519290
ATP13A2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519292
rs1057519292
ATP13A2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519293
rs1057519293
ATP13A2
A 0.700 CausalMutation CLINVAR

dbSNP: rs773246271
rs773246271
ATP13A2
A 0.700 CausalMutation CLINVAR