{{Rsnum
|rsid=193929364
|Chromosome=11
|position=17470109
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCC8
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000020288.1
|CLNALLE=1
|CLNDBN=Permanent neonatal diabetes mellitus
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1833104:606176:79134:99885
|CLNHGVS=NC_000011.9:g.17491656A>G
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1447
|Disease=Permanent neonatal diabetes mellitus
|FwdALT=C
|FwdREF=T
|GENEINFO=ABCC8:6833
|GENE_ID=6833
|GENE_NAME=ABCC8
|REF=A
|RSPOS=17491656
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=193929364
}}{{PMID Auto
|PMID=17668386
|Title=Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.
|OA=1
}}