{{Rsnum
|rsid=104894220
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DRD2
|position=113416935
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DRD2
}}{{omim
|id=126450
|rsnum=104894220
|variant=0001
}}{{ClinVar
|rsid=104894220
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=113287657
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=DRD2:1813
|GENE_NAME=DRD2
|GENE_ID=1813
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.113287657C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=126450.0001
|CLNSIG=5
|CLNCUI=C1834570
|CLNDBN=Myoclonic dystonia
|Disease=Myoclonic dystonia
|CLNACC=RCV000018259.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1414:C1834570:159900:36899:439732004
}}