{{Rsnum
|rsid=193922377
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYBPC3
|position=47343051
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922377
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=47364602
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47364602C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Disease=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Tags=RV;PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030279.1; RCV000035382.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1768:C0949658:83978005; CN169374
|GENEINFO=MYBPC3:4607
|GENE_ID=4607
|GENE_NAME=MYBPC3
}}{{PMID|18533079}} Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.

{{PMID|20414521}} [Study of mutations causing hypertrophic cardiomyopathy in a group of patients from Espirito Santo, Brazil].

{{PMID|20624503}} Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy.

{{PMID|20851114}} Development of a high resolution melting method for the detection of genetic variations in Long QT Syndrome.