{{Rsnum
|rsid=199865688
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MYBPC3
|position=47337496
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000035494.1; RCV000054796.3; RCV000054797.4
|CLNALLE=1
|CLNDBN=AllHighlyPenetrant; Left ventricular noncompaction 10; Familial hypertrophic cardiomyopathy 4
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM
|CLNDSDBID=CN169374; CN179849:615396:154:54260; NBK1768:C1861862:115197
|CLNHGVS=NC_000011.9:g.47359047C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600958.0024
|Disease=AllHighlyPenetrant; Left ventricular noncompaction 10; Familial hypertrophic cardiomyopathy 4
|FwdALT=T
|FwdREF=C
|GENEINFO=MYBPC3:4607
|GENE_ID=4607
|GENE_NAME=MYBPC3
|REF=C
|RSPOS=47359047
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199865688
}}