{{Rsnum
|rsid=80338717
|Gene=SLC25A13
|Chromosome=7
|position=96193032
|Orientation=minus
|GMAF=0.0004591
|Gene_s=SLC25A13
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=80338717
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=95822344
|CHROM=7
|GMAF=0.0005
|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.95822344C>T
|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=RCV000020707.1
|Tags=RV;PM;PMC;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1181:C1853942:605814:247598
|COMMON=0
}}{{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.
}}