{{Rsnum
|rsid=193922402
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ABCC8
|position=17395611
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922402
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=17417158
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17417158G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=familial hyperinsulinism
|Disease=familial hyperinsulinism
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029264.1
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK1375:CN043604
|GENEINFO=ABCC8:6833
|GENE_ID=6833
|GENE_NAME=ABCC8
}}{{PMID Auto
|PMID=9642650
|Title=Ions and genes in persistent hyperinsulinaemic hypoglycaemia in infancy: a commentary on the implications for tailoring treatment to disease pathogenesis.
}}