{{Rsnum
|rsid=121909374
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MYBPC3
|position=47342578
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYBPC3
}}{{omim
|id=600958
|rsnum=121909374
|variant=0006
}}{{ClinVar
|rsid=121909374
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=47364129
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MYBPC3:4607
|GENE_NAME=MYBPC3
|GENE_ID=4607
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47364129C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600958.0006
|CLNSIG=5
|CLNCUI=C1861862
|CLNDBN=Familial hypertrophic cardiomyopathy 4; Primary familial hypertrophic cardiomyopathy
|Disease=Familial hypertrophic cardiomyopathy 4; Primary familial hypertrophic cardiomyopathy
|CLNACC=RCV000009139.2; RCV000035424.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1768:C1861862:115197; NBK1768:C0949658:83978005
}}