{{Rsnum
|rsid=193922870
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=RYR1
|position=38579980
|Gene_s=RYR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000013862.22
|CLNALLE=1
|CLNDBN=Minicore myopathy with external ophthalmoplegia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1290:C1850674:255320:598
|CLNHGVS=NC_000019.9:g.39070620A>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=180901.0028
|Disease=Minicore myopathy with external ophthalmoplegia
|FwdALT=T
|FwdREF=A
|GENEINFO=RYR1:6261
|GENE_ID=6261
|GENE_NAME=RYR1
|REF=A
|RSPOS=39070620
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=193922870
}}{{PMID Auto
|PMID=16380615
|Title=Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.
}}