{{Rsnum
|rsid=80338716
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC25A13
|position=96193102
|Gene_s=SLC25A13
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338716
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=95822414
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SLC25A13:10165
|GENE_NAME=SLC25A13
|GENE_ID=10165
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.95822414G>A
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1181
|CLNSIG=5
|CLNCUI=C1853942
|CLNDBN=Neonatal intrahepatic cholestasis caused by citrin deficiency
|Disease=Neonatal intrahepatic cholestasis caused by citrin deficiency
|CLNACC=RCV000020705.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1181:C1853942:605814:247598
}}{{PMID Auto
|PMID=15050970
|Title=Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle.
}}