{{Rsnum
|rsid=80356620
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=KCNJ11
|position=17387593
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ11
}}{{omim
|id=600937
|rsnum=80356620
|variant=0016
}}{{ClinVar
|rsid=80356620
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=17409140
|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.17409140T>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1447; 600937.0016
|CLNSIG=5
|CLNCUI=C1833104
|CLNDBN=Diabetes mellitus, permanent neonatal, with neurologic features; Permanent neonatal diabetes mellitus
|Disease=Diabetes mellitus; Permanent neonatal diabetes mellitus
|CLNACC=RCV000009217.1; RCV000020353.1
|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=17652641
|Title=A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brain.
}}