{{Rsnum
|rsid=193922382
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYBPC3
|position=47334002
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922382
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=47355553
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47355553G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Disease=Primary familial hypertrophic cardiomyopathy; AllHighlyPenetrant
|Tags=RV;PM;OTHERKG;LSD
|CLNACC=RCV000030287.1; RCV000035542.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1768:C0949658:83978005; CN169374
|GENEINFO=MYBPC3:4607
|GENE_ID=4607
|GENE_NAME=MYBPC3
}}