{{Rsnum
|rsid=193929343
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KCNJ11
|position=17387595
|Gene_s=KCNJ11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=80356618
}}{{ClinVar
|rsid=193929343
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=17409142
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=0
|VP=050368000a11000002110100
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17409142C>A
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1447; NBK1447
|CLNSIG=5
|CLNCUI=C1833104; C1833104
|CLNDBN=Permanent neonatal diabetes mellitus
|Disease=Permanent neonatal diabetes mellitus
|CLNACC=SCV000040732.1; SCV000040732.1
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;OTH;OTHERKG;LSD;OM
}}{{PMID Auto
|PMID=16416420
|Title=Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.
}}

{{PMID Auto
|PMID=16670688
|Title=KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features.
}}