{{Rsnum
|rsid=193922323
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GCK
|position=44147809
|Gene_s=GCK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922323
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=44187408
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44187408A>G
|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=RCV000029911.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1447:C1841962:125851:552
|GENEINFO=GCK:2645
|GENE_ID=2645
|GENE_NAME=GCK
}}{{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=18399931
|Title=Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry.
}}

{{PMID Auto
|PMID=19790256
|Title=Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.
}}