{{Rsnum
|rsid=192057022
|Gene=MYL2
|Chromosome=12
|position=110913139
|Orientation=plus
|GMAF=0.0004591
|Gene_s=MYL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=192057022
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=111350943
|CHROM=12
|GMAF=0.0005
|dbSNPBuildID=135
|SSR=0
|SAO=1
|VP=0x050260000000000016100100
|GENEINFO=MYL2:4633
|GENE_NAME=MYL2
|GENE_ID=4633
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.111350943C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Disease=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9995; 0.0004591
|CLNACC=RCV000030324.1; RCV000036398.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1768:C0949658:83978005; CN169374
|COMMON=0
}}