{{Rsnum
|rsid=141028076
|Gene=SLC25A15
|Chromosome=13
|position=40807405
|Orientation=plus
|GMAF=0.0009183
|Gene_s=GPR82,SLC25A15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=G,T
|CAF=0.9991; 0.0009183
|CHROM=13
|CLNACC=RCV000031951.1
|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.41381541C>G
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK97260
|COMMON=0
|Disease=Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|FwdALT=G,T
|FwdREF=C
|GENEINFO=SLC25A15:10166; TPTE2P5:100616668
|GENE_ID=10166; 100616668
|GENE_NAME=SLC25A15; TPTE2P5
|REF=C
|RSPOS=41381541
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000000040016110100
|WGT=0
|dbSNPBuildID=134
|rsid=141028076
}}