{{Rsnum
|rsid=397509410
|Chromosome=14
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=DYNC1H1
|position=102032396
|Gene_s=DYNC1H1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000049270.1
|CLNALLE=1
|CLNDBN=Mental retardation, autosomal dominant 13
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3281202:614563
|CLNHGVS=NC_000014.8:g.102498733G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600112.0007
|Disease=Mental retardation
|FwdALT=T
|FwdREF=G
|REF=G
|RSPOS=102498733
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397509410
|GENEINFO=DYNC1H1:1778
|GENE_ID=1778
|GENE_NAME=DYNC1H1
}}