{{Rsnum
|rsid=72559723
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ABCC8
|position=17427124
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCC8
}}{{omim
|id=600509
|rsnum=72559723
|variant=0003
}}

{{ClinVar
|rsid=72559723
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=17448671
|CHROM=11
|dbSNPBuildID=130
|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.17448671C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=600509.0003
|CLNSIG=5
|CLNCUI=C1257959
|CLNDBN=Persistent hyperinsulinemic hypoglycemia of infancy; not provided
|Disease=Persistent hyperinsulinemic hypoglycemia of infancy; not provided
|CLNACC=RCV000009655.1; RCV000077845.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1375:C1257959:256450:276575:276598:360339005
}}

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