{{Rsnum
|rsid=80338727
|Chromosome=7
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SLC25A13
|position=96121695
|Gene_s=SLC25A13
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338727
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=95751007
|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; 2
|CLNHGVS=NC_000007.13:g.95751007C>A; NC_000007.13:g.95751007C>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=RCV000020703.1; RCV000020702.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1181:C1853942:605814:247598
}}{{PMID|11793471}} Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations.

{{PMID|11793471}} Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations.