{{Rsnum
|rsid=387906738
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DYNC1H1
|position=101980506
|Gene_s=DYNC1H1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=14
|CLNACC=RCV000022929.2; RCV000055662.1
|CLNALLE=1
|CLNDBN=Charcot-Marie-Tooth disease, axonal, type 2O; Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1285:C3280220:614228:284232; C1834690:158600:363447
|CLNHGVS=NC_000014.8:g.102446843A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600112.0001
|Disease=Charcot-Marie-Tooth disease; Spinal muscular atrophy
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=102446843
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906738
|GENEINFO=DYNC1H1:1778
|GENE_ID=1778
|GENE_NAME=DYNC1H1
}}