{{Rsnum
|rsid=121913618
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH3
|position=10641318
|Gene_s=MYH3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160720
|rsnum=121913618
|variant=0002
}}{{ClinVar
|rsid=121913618
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=10544635
|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.10544635G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160720.0002
|CLNSIG=5
|CLNCUI=C0265224
|CLNDBN=Freeman-Sheldon syndrome
|Disease=Freeman-Sheldon syndrome
|CLNACC=RCV000015201.20
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265224:193700:2053:52616002
}}