{{Rsnum
|rsid=121909342
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DCTN1
|position=74378104
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DCTN1
}}{{omim
|id=601143
|rsnum=121909342
|variant=0001
}}{{ClinVar
|rsid=121909342
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=74605231
|CHROM=2
|dbSNPBuildID=133
|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.74605231C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK47027; 601143.0001
|CLNSIG=5
|CLNCUI=C1843315; C1843315
|CLNDBN=Distal hereditary motor neuronopathy type 7B
|Disease=Distal hereditary motor neuronopathy type 7B
|CLNACC=RCV000008909.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK47027:C1843315:607641
}}