{{Rsnum
|rsid=2856655
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYBPC3
|position=47337534
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYBPC3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.9 | 99.1
| MEX | 0.0 | 1.7 | 98.3
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=600958
|rsnum=2856655
|variant=0015
}}

{{ClinVar
|rsid=2856655
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=47359085
|CHROM=11
|dbSNPBuildID=100
|SSR=0
|SAO=1
|VP=0x050060000000040503110100
|GENEINFO=MYBPC3:4607
|GENE_NAME=MYBPC3
|GENE_ID=4607
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47359085C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600958.0015
|CLNSIG=5
|CLNCUI=C1861862
|CLNDBN=Familial hypertrophic cardiomyopathy 4
|Disease=Familial hypertrophic cardiomyopathy 4
|CLNACC=RCV000009148.3
|Tags=RV;PM;VLD;HD;GNO;OTHERKG;PH3;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1768:C1861862:115197
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}