{{Rsnum
|rsid=387906408
|Chromosome=11
|position=17395892
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TCC)
|geno3=(TCC;TCC)
|Gene=ABCC8
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000009668.1
|CLNALLE=1
|CLNDBN=Persistent hyperinsulinemic hypoglycemia of infancy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1375:C1257959:256450:276575:276598:360339005
|CLNHGVS=NC_000011.9:g.17417439_17417441delGGA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600509.0014
|Disease=Persistent hyperinsulinemic hypoglycemia of infancy
|FwdREF=CCT
|REF=AGGA
|RSPOS=17417438
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906408
|GENEINFO=ABCC8:6833
|GENE_ID=6833
|GENE_NAME=ABCC8
}}