{{Rsnum
|rsid=267607190
|position=108564313
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ISCU
|Gene_s=ISCU
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=A
|CHROM=12
|CLNACC=RCV000000819.1
|CLNALLE=1
|CLNDBN=Myopathy with lactic acidosis, hereditary
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK5299:C1850718:255125:43115
|CLNHGVS=NC_000012.11:g.108958089G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611911.0002
|Disease=Myopathy with lactic acidosis
|FwdALT=A
|FwdREF=G
|GENEINFO=ISCU:23479
|GENE_ID=23479
|GENE_NAME=ISCU
|REF=G
|RSPOS=108958089
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607190
}}