{{Rsnum
|rsid=193922279
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GCK
|position=44153378
|Gene_s=GCK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922279
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=44192977
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44192977C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Maturity-onset diabetes of the young, type 2
|Disease=Maturity-onset diabetes of the young
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029859.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1447:C1841962:125851:552
|GENEINFO=GCK:2645
|GENE_ID=2645
|GENE_NAME=GCK
}}{{PMID Auto
|PMID=12627330
|Title=Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4alpha, GCK and HNF-1alpha.
}}

{{PMID Auto
|PMID=14517946
|Title=Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy.
}}

{{PMID Auto
|PMID=16602010
|Title=Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents.
}}

{{PMID Auto
|PMID=20337973
|Title=Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations.
}}