{{Rsnum
|rsid=121913658
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MYL2
|position=110913316
|Gene_s=MYL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=160781
|rsnum=121913658
|variant=0003
}}{{ClinVar
|rsid=121913658
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=111351120
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=MYL2:4633
|GENE_NAME=MYL2
|GENE_ID=4633
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.111351120G>C
|CLNSRC=Leiden Muscular Dystrophy pages (MYL2); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=MYL2_00007; 160781.0003
|CLNSIG=5
|CLNCUI=C1834460
|CLNDBN=Familial hypertrophic cardiomyopathy 10
|Disease=Familial hypertrophic cardiomyopathy 10
|CLNACC=RCV000015110.24
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1768:C1834460:608758
}}{{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.
}}