{{Rsnum
|rsid=202247803
|Chromosome=13
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TTC)
|geno3=(TTC;TTC)
|Gene=GPR82
|position=40807403
|Gene_s=GPR82,SLC25A15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=13
|CLNACC=RCV000006358.3
|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.41381539_41381541delTTC
|CLNSIG=5
|CLNSRC=GTR; GeneReviews; OMIM Allelic Variant
|CLNSRCID=GTR000204863; NBK97260; 603861.0001
|Disease=Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|FwdREF=TTC
|GENEINFO=SLC25A15:10166; TPTE2P5:100616668
|GENE_ID=10166; 100616668
|GENE_NAME=SLC25A15; TPTE2P5
|REF=TTTC
|RSPOS=41381529
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050160000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=202247803
}}