{{Rsnum
|rsid=371401403
|Chromosome=11
|position=47335996
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYBPC3
|Gene_s=MYBPC3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=11
|CLNACC=RCV000054802.2; RCV000023054.2; RCV000035516.1
|CLNALLE=1; 2
|CLNDBN=Left ventricular noncompaction 10; Familial hypertrophic cardiomyopathy 4; AllHighlyPenetrant
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=CN179849:615396:154:54260; NBK1768:C1861862:115197; CN169374
|CLNHGVS=NC_000011.9:g.47357547G>A; NC_000011.9:g.47357547G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600958.0027; 600958.0022
|Disease=Left ventricular noncompaction 10; Familial hypertrophic cardiomyopathy 4; AllHighlyPenetrant
|FwdALT=A,T
|FwdREF=G
|REF=G
|RSPOS=47357547
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=371401403
|GENEINFO=MYBPC3:4607
|GENE_ID=4607
|GENE_NAME=MYBPC3
}}