{{Rsnum
|rsid=151344624
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TTC)
|geno3=(TTC;TTC)
|Gene=ABCC8
|position=17395889
|Gene_s=ABCC8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=151344624
|Reversed=1
|FwdREF=TCT
|FwdALT=TTCT,T
|REF=AGAA
|ALT=A
|RSPOS=17417435
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=0
|VP=0x050160000000000002110200
|GENEINFO=ABCC8:6833
|GENE_NAME=ABCC8
|GENE_ID=6833
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17417436_17417438delGAA
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600509.0006
|CLNSIG=5
|CLNCUI=C1257959
|CLNDBN=Persistent hyperinsulinemic hypoglycemia of infancy
|Disease=Persistent hyperinsulinemic hypoglycemia of infancy
|CLNACC=RCV000009660.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1375:C1257959:256450:276575:276598:360339005
}}