{{Rsnum
|rsid=104894430
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC25A15
|position=40799080
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GPR82,SLC25A15
}}{{omim
|id=603861
|rsnum=104894430
|variant=0004
}}{{ClinVar
|rsid=104894430
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=41373216
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050360000000000002110100
|GENEINFO=SLC25A15:10166; TPTE2P5:100616668
|GENE_NAME=SLC25A15; TPTE2P5
|GENE_ID=10166; 100616668
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.41373216G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK97260; 603861.0004
|CLNSIG=5
|CLNCUI=C0268540
|CLNDBN=Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|Disease=Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|CLNACC=RCV000006361.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK97260:C0268540:238970:415:30287008
}}