{{Rsnum
|rsid = 28936370
|Gene = ABCC8
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=11
|position=17396980
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCC8
}}{{omim
|desc=HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1
|id=600509
|rsnum=28936370
|variant=0008
}}

{{ neighbor
| rsid = 757110
| distance = 50
}}

{{omim
|id=600509
|rsnum=28936370
|variant=0012
}}

{{ClinVar
|rsid=28936370
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=17418527
|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; 2
|CLNHGVS=NC_000011.9:g.17418527C>G; NC_000011.9:g.17418527C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000009662.1; RCV000009666.1
|CLNDBN=Persistent hyperinsulinemic hypoglycemia of infancy; Leucine-induced hypoglycemia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1375:C1257959:256450:276575:276598:360339005; C0271714:240800:62151007
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600509.0008; 600509.0012
|Disease=Persistent hyperinsulinemic hypoglycemia of infancy; Leucine-induced hypoglycemia
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}