{{Rsnum
|rsid=193929360
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCC8
|position=17474919
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C,G
|CHROM=11
|CLNACC=RCV000009681.1; RCV000020285.1
|CLNALLE=1; 2
|CLNDBN=Permanent neonatal diabetes mellitus
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1833104:606176:79134:99885
|CLNHGVS=NC_000011.9:g.17496466A>C; NC_000011.9:g.17496466A>G
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1447; 600509.0026
|Disease=Permanent neonatal diabetes mellitus
|FwdALT=C,G
|FwdREF=T
|GENEINFO=ABCC8:6833
|GENE_ID=6833
|GENE_NAME=ABCC8
|REF=A
|RSPOS=17496466
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=193929360
}}{{PMID Auto
|PMID=17668386
|Title=Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.
|OA=1
}}