{{Rsnum
|rsid=104894369
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYL2
|position=110914287
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYL2
}}{{omim
|id=160781
|rsnum=104894369
|variant=0004
}}{{ClinVar
|rsid=104894369
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=111352091
|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.111352091C>T
|CLNSRC=Leiden Muscular Dystrophy pages (MYL2); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=MYL2_00005; 160781.0004
|CLNSIG=5
|CLNCUI=C1834460
|CLNDBN=Familial hypertrophic cardiomyopathy 10; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 10; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000015111.24; RCV000036383.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C1834460:608758; NBK1768:C0949658:83978005
}}{{PMID Auto
|PMID=9535554
|Title=Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.
}}

{{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=12707239
|Title=Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
}}

{{PMID Auto
|PMID=12818575
|Title=Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden.
}}

{{PMID Auto
|PMID=18533079
|Title=Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.
}}