{{Rsnum
|rsid=193929374
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GCK
|position=44145617
|Gene_s=GCK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=7
|CLNACC=RCV000020165.1
|CLNALLE=1
|CLNDBN=Permanent neonatal diabetes mellitus
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1833104:606176:79134:99885
|CLNHGVS=NC_000007.13:g.44185216G>A
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1447
|Disease=Permanent neonatal diabetes mellitus
|FwdALT=T
|FwdREF=C
|GENEINFO=GCK:2645
|GENE_ID=2645
|GENE_NAME=GCK
|REF=G
|RSPOS=44185216
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=193929374
}}{{PMID Auto
|PMID=14578306
|Title=Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway.
}}