{{Rsnum
|rsid=104893749
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYL3
|position=46859495
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYL3
}}{{omim
|id=160790
|rsnum=104893749
|variant=0002
}}{{ClinVar
|rsid=104893749
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=46900985
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=MYL3:4634
|GENE_NAME=MYL3
|GENE_ID=4634
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.46900985C>T
|CLNSRC=Leiden Muscular Dystrophy pages (MYL3); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=MYL3_00003; 160790.0002
|CLNSIG=5
|CLNCUI=C1837471
|CLNDBN=Familial hypertrophic cardiomyopathy 8; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 8; AllHighlyPenetrant
|CLNACC=RCV000015106.20; RCV000036025.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1768:C1837471:608751; CN169374
}}{{PMID Auto
|PMID=8673105
|Title=Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.
}}