{{Rsnum
|rsid=143139258
|Orientation=plus
|Chromosome=12
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYL2
|position=110913097
|Gene_s=MYL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=12
|CLNACC=RCV000036404.1
|CLNALLE=1
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|CLNHGVS=NC_000012.11:g.111350901T>G
|CLNORIGIN=1
|CLNSIG=4
|Disease=Primary familial hypertrophic cardiomyopathy
|FwdALT=G
|FwdREF=T
|GENEINFO=MYL2:4633
|GENE_ID=4633
|GENE_NAME=MYL2
|REF=T
|RSPOS=111350901
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;VLD;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000040002100100
|WGT=0
|dbSNPBuildID=134
|rsid=143139258
}}{{PMID Auto
|PMID=18533079
|Title=Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.
}}