{{Rsnum
|rsid=104894368
|Gene=MYL2
|Chromosome=12
|position=110919133
|Orientation=minus
|GMAF=0.0
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MYL2
}}{{omim
|id=160781
|rsnum=104894368
|variant=0002
}}{{ClinVar
|rsid=104894368
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=111356937
|CHROM=12
|GMAF=0
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000016110100
|GENEINFO=MYL2:4633
|GENE_NAME=MYL2
|GENE_ID=4633
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.111356937C>T
|CLNSRC=Leiden Muscular Dystrophy pages (MYL2); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=MYL2_00003; 160781.0002
|CLNSIG=5
|CLNCUI=C1834460
|CLNDBN=Familial hypertrophic cardiomyopathy 10
|Disease=Familial hypertrophic cardiomyopathy 10
|CLNACC=RCV000015109.24
|Tags=RV;PM;PMC;S3D;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1768:C1834460:608758
|COMMON=0
}}{{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.
}}

{{PMID Auto
|PMID=12404107
|Title=Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.
}}

{{PMID Auto
|PMID=21896538
|Title=Genetic basis of end-stage hypertrophic cardiomyopathy.
}}