{{Rsnum
|rsid=121908461
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYOT
|position=137870767
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC101928005,MYOT
}}{{omim
|id=604103
|rsnum=121908461
|variant=0006
}}{{ClinVar
|rsid=121908461
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=137206456
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MYOT:9499
|GENE_NAME=MYOT
|GENE_ID=9499
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.137206456C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604103.0006
|CLNSIG=5
|CLNCUI=C1866785
|CLNDBN=Spheroid body myopathy
|Disease=Spheroid body myopathy
|CLNACC=RCV000006196.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1866785:182920:268129
}}