{{Rsnum
|rsid=121434590
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MYH8
|position=10406924
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MYH8
}}{{omim
|id=160741
|rsnum=121434590
|variant=0001
}}{{ClinVar
|rsid=121434590
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=10310241
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MYH8:4626
|GENE_NAME=MYH8
|GENE_ID=4626
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.10310241C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=160741.0001
|CLNSIG=5
|CLNCUI=C1837245; C0265226
|CLNDBN=Carney complex variant; Hecht syndrome
|Disease=Carney complex variant; Hecht syndrome
|CLNACC=RCV000015197.24; RCV000015198.24
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1837245:608837; C0265226:158300:3377:8757006
}}