{{Rsnum
|rsid=193929336
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNJ11
|position=17387943
|Gene_s=KCNJ11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=80356611
}}{{ClinVar
|rsid=193929336
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=17409490
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=0
|VP=050368080811000002110100
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.17409490C>G
|CLNSRC=OMIM Allelic Variant; GeneReviews
|CLNORIGIN=0
|CLNSRCID=600937.0006; NBK1447
|CLNSIG=5
|CLNCUI=C1833104; C1833104
|CLNDBN=Permanent neonatal diabetes mellitus
|Disease=Permanent neonatal diabetes mellitus
|CLNACC=SCV000029423.1; SCV000040724.1
|Tags=RV;PM;PMC;S3D;SLO;NSM;INT;OTH;OTHERKG;LSD;OM
}}{{PMID|15580558}} KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.