{{Rsnum
|rsid=121913653
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYH7
|position=23429040
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160760
|rsnum=121913653
|variant=0036
}}{{ClinVar
|rsid=121913653
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=23898249
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYH7:4625
|GENE_NAME=MYH7
|GENE_ID=4625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.23898249G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000015180.24; RCV000035714.1
|CLNDBN=Laing distal myopathy; AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=160760.0036
|Disease=Laing distal myopathy; AllHighlyPenetrant
}}