{{Rsnum
|rsid=104894363
|Gene=MYL2
|Chromosome=12
|position=110919160
|Orientation=plus
|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=104894363
|variant=0001
}}{{ClinVar
|rsid=104894363
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=111356964
|CHROM=12
|GMAF=0
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000040016110100
|GENEINFO=MYL2:4633
|GENE_NAME=MYL2
|GENE_ID=4633
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.111356964C>T
|CLNSRC=Leiden Muscular Dystrophy pages (MYL2); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=MYL2_00001; 160781.0001
|CLNSIG=5
|CLNCUI=C1834460
|CLNDBN=Familial hypertrophic cardiomyopathy 10; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 10; AllHighlyPenetrant
|CLNACC=RCV000015108.24; RCV000036401.1
|Tags=RV;PM;PMC;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1768:C1834460:608758; CN169374
|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=11748309
|Title=Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.
|OA=1
}}

{{PMID Auto
|PMID=15483641
|Title=One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.
}}