{{Rsnum
|rsid=121913619
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH3
|position=10650374
|Gene_s=MYH3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160720
|rsnum=121913619
|variant=0003
}}{{ClinVar
|rsid=121913619
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=10553691
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYH3:4621
|GENE_NAME=MYH3
|GENE_ID=4621
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.10553691G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160720.0003
|CLNSIG=5
|CLNCUI=C0265224; C1834523
|CLNDBN=Freeman-Sheldon syndrome; Distal arthrogryposis type 2B
|Disease=Freeman-Sheldon syndrome; Distal arthrogryposis type 2B
|CLNACC=RCV000015202.24; RCV000015203.24
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C0265224:193700:2053:52616002; C1834523:601680:1147
}}