{{Rsnum
|rsid=193922391
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYL3
|position=46858413
|Gene_s=MYL3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922391
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=46899903
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050260000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.46899903T>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|Disease=Primary familial hypertrophic cardiomyopathy
|Tags=RV;PM;S3D;OTHERKG;LSD
|CLNACC=RCV000030327.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
|GENEINFO=MYL3:4634
|GENE_ID=4634
|GENE_NAME=MYL3
}}