{{Rsnum
|rsid=193922380
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MYBPC3
|position=47335077
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922380
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=47356628
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47356628G>C
|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=RCV000030285.1; RCV000035534.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1768:C0949658:83978005; CN169374
|GENEINFO=MYBPC3:4607
|GENE_ID=4607
|GENE_NAME=MYBPC3
}}{{PMID|18957093|OA=1
}} Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene.

{{PMID|20433692|OA=1
}} Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy.