{{Rsnum
|rsid=199474809
|Orientation=minus
|Chromosome=12
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYL2
|position=110914290
|Gene_s=MYL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=12
|CLNACC=RCV000036384.1
|CLNALLE=1
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|CLNHGVS=NC_000012.11:g.111352094C>T
|CLNORIGIN=1
|CLNSIG=4
|Disease=Primary familial hypertrophic cardiomyopathy
|FwdALT=A
|FwdREF=G
|GENEINFO=MYL2:4633
|GENE_ID=4633
|GENE_NAME=MYL2
|REF=C
|RSPOS=111352094
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199474809
}}{{PMID Auto
|PMID=21823217
|Title=Furthering the link between the sarcomere and primary cardiomyopathies: restrictive cardiomyopathy associated with multiple mutations in genes previously associated with hypertrophic or dilated cardiomyopathy.
|OA=1
}}