{{Rsnum
|rsid=193922311
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GCK
|position=44149834
|Gene_s=GCK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922311
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=44189433
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44189433A>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=RCV000029896.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1447:C1841962:125851:552
|GENEINFO=GCK:2645
|GENE_ID=2645
|GENE_NAME=GCK
}}{{PMID Auto
|PMID=17573900
|Title=Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain.
}}

{{PMID Auto
|PMID=17937063
|Title=Four novel mutations, including the first gross deletion in TCF1, identified in HNF-4alpha, GCK and TCF1 in patients with MODY in Israel.
}}