{{Rsnum
|rsid=121908107
|Gene=MYLK2
|Chromosome=20
|position=31820333
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYLK2
}}{{omim
|id=606566
|rsnum=121908107
|variant=0001
}}{{ClinVar
|rsid=121908107
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=30408136
|CHROM=20
|GMAF=0.0009
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=MYLK2:85366
|GENE_NAME=MYLK2
|GENE_ID=85366
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.30408136C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606566.0001
|CLNSIG=5
|CLNCUI=CN068809
|CLNDBN=Cardiomyopathy, hypertrophic, midventricular, digenic
|Disease=Cardiomyopathy
|CLNACC=RCV000004465.1
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=MedGen
|CLNDSDBID=CN068809
|COMMON=1
}}