{{Rsnum
|rsid=80356610
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNJ11
|position=17387968
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ11
}}{{omim
|id=600937
|rsnum=80356610
|variant=0012
}}{{ClinVar
|rsid=80356610
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=17409515
|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.17409515A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1447; 600937.0012
|CLNSIG=5
|CLNCUI=C1864623; C1833104
|CLNDBN=Transient neonatal diabetes mellitus 3; DIABETES MELLITUS, TYPE II, AUTOSOMAL DOMINANT; Permanent neonatal diabetes mellitus
|Disease=Transient neonatal diabetes mellitus 3; DIABETES MELLITUS; Permanent neonatal diabetes mellitus
|CLNACC=RCV000009211.1; RCV000009212.1; RCV000020347.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1864623:610582; C0342277; NBK1447:C1833104:606176:79134:99885
}}{{PMID Auto
|PMID=15784703
|Title=The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus.
}}