{{Rsnum
|rsid=121917767
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=UCHL1
|position=41260751
|Gene_s=UCHL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=191342
|rsnum=121917767
|variant=0001
}}{{ClinVar
|rsid=121917767
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=41262768
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=UCHL1:7345
|GENE_NAME=UCHL1
|GENE_ID=7345
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.41262768C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=191342.0001
|CLNSIG=5
|CLNCUI=C1860619
|CLNDBN=Parkinson disease 5
|Disease=Parkinson disease 5
|CLNACC=RCV000013091.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1223:C3150899:613643:2828
}}