{{Rsnum
|rsid=193929373
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GCK
|position=44147723
|Gene_s=GCK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=7
|CLNACC=RCV000020168.1
|CLNALLE=1
|CLNDBN=Permanent neonatal diabetes mellitus
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1833104:606176:79134:99885
|CLNHGVS=NC_000007.13:g.44187322C>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1447
|Disease=Permanent neonatal diabetes mellitus
|FwdALT=A
|FwdREF=G
|GENEINFO=GCK:2645
|GENE_ID=2645
|GENE_NAME=GCK
|REF=C
|RSPOS=44187322
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=193929373
}}{{PMID Auto
|PMID=14578306
|Title=Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway.
}}