{{Rsnum
|rsid=137853967
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ATP13A2
|position=16986864
|Gene_s=ATP13A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=137853967
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=17313359
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000a01000002110100
|GENEINFO=ATP13A2:23400
|GENE_NAME=ATP13A2
|GENE_ID=23400
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.10:g.17313359A>C
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=606693
|CLNDBN=Parkinson disease 9
|Tags=RV;PM;PMC;NSM;REF;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=137853967
}}