{{Rsnum
|rsid=80356640
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ABCC8
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=17461778
}}{{ClinVar
|ALT=A,T
|CHROM=11
|CLNACC=RCV000020289.1
|CLNALLE=2
|CLNDBN=Permanent neonatal diabetes mellitus
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1833104:606176:79134:99885
|CLNHGVS=NC_000011.9:g.17483325G>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1447
|Disease=Permanent neonatal diabetes mellitus
|FwdALT=A,T
|FwdREF=C
|GENEINFO=ABCC8:6833
|GENE_ID=6833
|GENE_NAME=ABCC8
|REF=G
|RSPOS=17483325
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=80356640
}}{{PMID Auto
|PMID=17446535
|Title=Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood.
}}

{{PMID Auto
|PMID=17668386
|Title=Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.
|OA=1
}}