{{Rsnum
|rsid=193929363
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCC8
|position=17470119
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=80356637
}}{{ClinVar
|rsid=193929363
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=17491666
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=0
|VP=050168000a11000002110100
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17491666A>G
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1447; NBK1447
|CLNSIG=5
|CLNCUI=C1833104; C1833104
|CLNDBN=Permanent neonatal diabetes mellitus
|Disease=Permanent neonatal diabetes mellitus
|CLNACC=SCV000040645.1; SCV000040645.1
|Tags=RV;PM;PMC;SLO;NSM;REF;OTH;OTHERKG;LSD;OM
}}{{PMID Auto
|PMID=16613899
|Title=A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.
}}