{{Rsnum
|rsid=36211723
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYBPC3
|position=47338520
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=36211723
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=47360071
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050268000000000502100100
|GENEINFO=MYBPC3:4607
|GENE_NAME=MYBPC3
|GENE_ID=4607
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47360071C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy
|Disease=Primary familial hypertrophic cardiomyopathy
|Tags=RV;PM;PMC;S3D;HD;GNO;OTHERKG;LSD
|CLNACC=RCV000030282.2
|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=16858239
|Title=A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.
}}

{{PMID Auto
|PMID=18273486
|Title=MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India.
|OA=1
}}

{{PMID Auto
|PMID=18533079
|Title=Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}