{{Rsnum
|rsid=80356663
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=INS
|position=2160901
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=INS,INS-IGF2
}}{{omim
|id=176730
|rsnum=80356663
|variant=0012
}}{{ClinVar
|rsid=80356663
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=2182131
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=INS:3630; INS-IGF2:723961
|GENE_NAME=INS; INS-IGF2
|GENE_ID=3630; 723961
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.2182131G>A; NC_000011.9:g.2182131G>T
|CLNSRC=GeneReviews; OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1; 0
|CLNSRCID=NBK1447; 176730.0012; VAR_063723
|CLNSIG=5
|CLNCUI=C1833104
|CLNDBN=Neonatal diabetes mellitus; Permanent neonatal diabetes mellitus
|Disease=Neonatal diabetes mellitus; Permanent neonatal diabetes mellitus
|CLNACC=RCV000030071.1; RCV000014320.18
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C0158981:49817004; NBK1447:C1833104:606176:79134:99885
}}{{PMID Auto
|PMID=17855560
|Title=Insulin gene mutations as a cause of permanent neonatal diabetes.
|OA=1
}}{{PMID Auto
|PMID=17047922
|Title=Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene.
}}

{{PMID Auto
|PMID=18171712
|Title=Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group.
}}