{{Rsnum
|rsid=187830361
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYBPC3
|position=47337729
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=187830361
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=47359280
|CHROM=11
|dbSNPBuildID=135
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|GENEINFO=MYBPC3:4607
|GENE_NAME=MYBPC3
|GENE_ID=4607
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.47359280A>G
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|Disease=Primary familial hypertrophic cardiomyopathy
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030283.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C0949658:83978005
}}{{PMID Auto
|PMID=15519027
|Title=Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.
}}

{{PMID Auto
|PMID=19808356
|Title=Expression patterns of cardiac myofilament proteins: genomic and protein analysis of surgical myectomy tissue from patients with obstructive hypertrophic cardiomyopathy.
|OA=1
}}