{{Rsnum
|rsid=202247807
|Chromosome=13
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC25A15
|position=40809584
|Gene_s=GPR82,MIR621,SLC25A15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=13
|CLNACC=RCV000031955.1
|CLNALLE=1
|CLNDBN=Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK97260:C0268540:238970:415:30287008
|CLNHGVS=NC_000013.10:g.41383720C>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK97260
|Disease=Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=SLC25A15:10166; MIR621:693206; TPTE2P5:100616668
|GENE_ID=10166; 693206; 100616668
|GENE_NAME=SLC25A15; MIR621; TPTE2P5
|REF=C
|RSPOS=41383720
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=202247807
}}