{{Rsnum
|rsid=121908970
|Gene=MYO15A
|Chromosome=17
|position=18148133
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYO15A
}}{{omim
|id=602666
|rsnum=121908970
|variant=0007
}}{{ClinVar
|rsid=121908970
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=18051447
|CHROM=17
|GMAF=0.0014
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040016110100
|GENEINFO=MYO15A:51168
|GENE_NAME=MYO15A
|GENE_ID=51168
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.18051447C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNACC=RCV000007371.1; RCV000038978.1
|CLNDBN=Deafness, with smith-magenis syndrome; AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602666.0007
|COMMON=1
|Disease=Deafness; AllHighlyPenetrant
}}