{{Rsnum
|rsid=387906681
|Chromosome=19
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=RYR1
|position=38489355
|Gene_s=RYR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=19
|CLNACC=RCV000022757.1
|CLNALLE=1
|CLNDBN=Minicore myopathy with external ophthalmoplegia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1290:C1850674:255320:598
|CLNHGVS=NC_000019.9:g.38979995_38979996delAG
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=180901.0035
|Disease=Minicore myopathy with external ophthalmoplegia
|FwdREF=AG
|REF=AAG
|RSPOS=38979992
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906681
|GENEINFO=RYR1:6261
|GENE_ID=6261
|GENE_NAME=RYR1
}}