{{Rsnum
|rsid=193922401
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ABCC8
|position=17395914
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922401
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=17417461
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17417461C>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Neonatal diabetes mellitus
|Disease=Neonatal diabetes mellitus
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029262.1
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0158981:49817004
|GENEINFO=ABCC8:6833
|GENE_ID=6833
|GENE_NAME=ABCC8
}}{{PMID Auto
|PMID=17919176
|Title=Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period.
}}

{{PMID Auto
|PMID=18025408
|Title=Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations.
}}

{{PMID Auto
|PMID=18025464
|Title=Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes.
|OA=1
}}

{{PMID Auto
|PMID=18436707
|Title=Neonatal diabetes mellitus.
|OA=1
}}

{{PMID Auto
|PMID=19095654
|Title=17beta-Estradiol modulates apoptosis in pancreatic beta-cells by specific involvement of the sulfonylurea receptor (SUR) isoform SUR1.
}}