{{Rsnum
|rsid=199474703
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYL3
|position=46860702
|Gene_s=MYL3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=3
|CLNACC=RCV000024468.1; RCV000036020.1
|CLNALLE=1
|CLNDBN=not provided; Primary familial hypertrophic cardiomyopathy
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|CLNHGVS=NC_000003.11:g.46902192C>T
|CLNORIGIN=1
|CLNSIG=4
|CLNSRC=Leiden Muscular Dystrophy pages (MYL3)
|CLNSRCID=MYL3_00005
|Disease=not provided; Primary familial hypertrophic cardiomyopathy
|FwdALT=A
|FwdREF=G
|GENEINFO=MYL3:4634
|GENE_ID=4634
|GENE_NAME=MYL3
|REF=C
|RSPOS=46902192
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199474703
}}{{PMID Auto
|PMID=18409188
|Title=A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy.
}}