{{Rsnum
|rsid=397516407
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MYL2
|position=110911090
|Gene_s=MYL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=12
|CLNACC=RCV000036409.1
|CLNALLE=1
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|CLNHGVS=NC_000012.11:g.111348894T>G
|CLNSIG=4
|Disease=Primary familial hypertrophic cardiomyopathy
|FwdALT=C
|FwdREF=A
|GENEINFO=MYL2:4633
|GENE_ID=4633
|GENE_NAME=MYL2
|REF=T
|RSPOS=111348894
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=138
|rsid=397516407
}}