{{Rsnum
|rsid=397514751
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYBPC3
|position=47332095
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=11
|CLNACC=RCV000054798.3; RCV000035617.1
|CLNALLE=1; 2
|CLNDBN=Left ventricular noncompaction 10; AllHighlyPenetrant
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet; MedGen
|CLNDSDBID=CN179849:615396:154:54260; CN169374
|CLNHGVS=NC_000011.9:g.47353646C>A; NC_000011.9:g.47353646C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600958.0025
|Disease=Left ventricular noncompaction 10; AllHighlyPenetrant
|FwdALT=A,T
|FwdREF=G
|GENEINFO=MYBPC3:4607
|GENE_ID=4607
|GENE_NAME=MYBPC3
|REF=C
|RSPOS=47353646
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514751
}}