{{Rsnum
|rsid=80338722
|Gene=SLC25A13
|Chromosome=7
|position=96184276
|Orientation=minus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SLC25A13
}}{{omim
|id=603859
|rsnum=80338722
|variant=0002
}}{{ClinVar
|rsid=80338722
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=95813588
|CHROM=7
|GMAF=0.0014
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000016110100
|GENEINFO=SLC25A13:10165
|GENE_NAME=SLC25A13
|GENE_ID=10165
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.95813588C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1181; 603859.0002
|CLNSIG=5
|CLNCUI=C1863844; C1853942; C1863844
|CLNDBN=Citrullinemia type II; Neonatal intrahepatic cholestasis caused by citrin deficiency
|Disease=Citrullinemia type II; Neonatal intrahepatic cholestasis caused by citrin deficiency
|CLNACC=RCV000006369.1; RCV000006370.1
|Tags=RV;PM;PMC;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1181:C1863844:603471:247585; NBK1181:C1853942:605814:247598
|COMMON=1
}}{{PMID Auto
|PMID=10369257
|Title=The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein.
}}

{{PMID Auto
|PMID=11281457
|Title=Neonatal presentation of adult-onset type II citrullinemia.
}}

{{PMID Auto
|PMID=12424587
|Title=Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation.
}}