{{Rsnum
|rsid=80356654
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=GCK
|position=44149810
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GCK
}}{{omim
|id=138079
|rsnum=80356654
|variant=0010
}}{{ClinVar
|rsid=80356654
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=44189409
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=GCK:2645
|GENE_NAME=GCK
|GENE_ID=2645
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44189409A>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1447; 138079.0010
|CLNSIG=5
|CLNCUI=C1833104
|CLNDBN=Permanent neonatal diabetes mellitus; MATURITY-ONSET DIABETES OF THE YOUNG, TYPE II
|Disease=Permanent neonatal diabetes mellitus; MATURITY-ONSET DIABETES OF THE YOUNG
|CLNACC=RCV000017521.27; RCV000017522.26
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1833104:606176:79134:99885
}}{{PMID|11372010}} Neonatal diabetes mellitus due to complete glucokinase deficiency.