{{Rsnum
|rsid=193922405
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ABCC8
|position=17394360
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922405
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=17415907
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17415907C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Persistent hyperinsulinemic hypoglycemia of infancy
|Disease=Persistent hyperinsulinemic hypoglycemia of infancy
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029267.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1375:C1257959:256450:276575:276598:360339005
|GENEINFO=ABCC8:6833
|GENE_ID=6833
|GENE_NAME=ABCC8
}}{{PMID Auto
|PMID=20573158
|Title=Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia.
|OA=1
}}