{{Rsnum
|rsid=121918227
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ATP13A2
|position=16996008
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP13A2
}}{{omim
|id=610513
|rsnum=121918227
|variant=0004
}}{{ClinVar
|rsid=121918227
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=16996008
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=ATP13A2:23400
|GENE_NAME=ATP13A2
|GENE_ID=23400
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.16996008C>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_022089.2:c.1510G>C; 610513.0004
|CLNSIG=5
|CLNCUI=C1847640
|CLNDBN=Parkinson disease 9
|Disease=Parkinson disease 9
|CLNACC=RCV000001280.2
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1223:C1847640:606693:ORPHA314632
}}