{{Rsnum
|rsid=104893873
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SLC25A4
|position=185144992
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC25A4
}}{{omim
|id=103220
|rsnum=104893873
|variant=0001
}}{{ClinVar
|rsid=104893873
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=186066146
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SLC25A4:291
|GENE_NAME=SLC25A4
|GENE_ID=291
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.186066146G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=103220.0001
|CLNSIG=5
|CLNCUI=C1836460
|CLNDBN=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
|Disease=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
|CLNACC=RCV000019907.25
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1836460:609283
}}