{{Rsnum
|rsid=80356617
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KCNJ11
|position=17387916
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ11
}}{{omim
|id=600937
|rsnum=80356617
|variant=0005
}}{{ClinVar
|rsid=80356617
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=17409463
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KCNJ11:3767
|GENE_NAME=KCNJ11
|GENE_ID=3767
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17409463A>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1447; 600937.0005
|CLNSIG=5
|CLNCUI=C1833104
|CLNDBN=Diabetes mellitus, permanent neonatal, with neurologic features; Permanent neonatal diabetes mellitus
|Disease=Diabetes mellitus; Permanent neonatal diabetes mellitus
|CLNACC=RCV000009204.1; RCV000020350.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1833102; NBK1447:C1833104:606176:79134:99885
}}{{PMID Auto
|PMID=15115830
|Title=Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.
}}

{{PMID Auto
|PMID=15583126
|Title=Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.
|OA=1
}}

{{PMID Auto
|PMID=16123337
|Title=Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy.
}}