{{Rsnum
|rsid=137853968
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=ATP13A2
|position=16986615
|Gene_s=ATP13A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=137853968
|Reversed=1
|FwdREF=C
|FwdALT=
|REF=AG
|ALT=A
|RSPOS=17313109
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050068081201000002110200
|GENEINFO=ATP13A2:23400
|GENE_NAME=ATP13A2
|GENE_ID=23400
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000001.10:g.17313110delG
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=606693
|CLNDBN=Parkinson disease 9
|Tags=RV;PM;PMC;NSF;REF;INT;OTHERKG;LSD;OM
|CLNDSDB=OMIM
|CLNDSDBID=606693
|Disease=Parkinson disease 9
}}{{PMID Auto
|PMID=21542062
|Title=Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism.
}}
{{omim
|id=606693
|rsnum=137853968
}}