{{Rsnum
|rsid=72466485
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DCTN1
|position=74378068
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DCTN1
}}{{omim
|id=601143
|rsnum=72466485
|variant=0006
}}{{ClinVar
|rsid=72466485
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=74605195
|CHROM=2
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=DCTN1:1639
|GENE_NAME=DCTN1
|GENE_ID=1639
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.74605195C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK47027; 601143.0006
|CLNSIG=5
|CLNCUI=C1868594; C1868594
|CLNDBN=Perry syndrome
|Disease=Perry syndrome
|CLNACC=RCV000008914.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK47027:C1868594:168605:178509
}}