{{Rsnum
|rsid=121913635
|Chromosome=14
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MYH7
|position=23429278
|Gene_s=MYH7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=121913624
}}{{omim
|id=160760
|variant=0014
|rsnum=121913635
}}{{ClinVar
|rsid=121913635
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=23898487
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=050260000a11000002110100
|GENEINFO=MYH7:4625
|GENE_NAME=MYH7
|GENE_ID=4625
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.23898487C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160760.0014
|CLNSIG=5
|CLNCUI=CN030093
|CLNDBN=Familial hypertrophic cardiomyopathy 1
|Disease=Familial hypertrophic cardiomyopathy 1
|CLNACC=SCV000035414.1
|Tags=RV;PM;S3D;NSM;REF;OTH;OTHERKG;LSD;OM
}}