{{Rsnum
|rsid = 28938469
|Gene = ABCC8
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=17395659
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCC8
}}{{omim
|desc=HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1
|id=600509
|rsnum=28938469
|variant=0009
}}

{{ClinVar
|rsid=28938469
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=17417206
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ABCC8:6833
|GENE_NAME=ABCC8
|GENE_ID=6833
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17417206G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600509.0009
|CLNSIG=5
|CLNCUI=C1257959
|CLNDBN=Persistent hyperinsulinemic hypoglycemia of infancy
|Disease=Persistent hyperinsulinemic hypoglycemia of infancy
|CLNACC=RCV000009663.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1375:C1257959:256450:276575:276598:360339005
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}