{{Rsnum
|rsid=104894012
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GCK
|position=44145171
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GCK
}}{{omim
|id=138079
|rsnum=104894012
|variant=0009
}}{{ClinVar
|rsid=104894012
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=44184770
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GCK:2645
|GENE_NAME=GCK
|GENE_ID=2645
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44184770C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=138079.0009
|CLNSIG=5
|CLNCUI=C1865290
|CLNDBN=Hyperinsulinemic hypoglycemia familial 3
|Disease=Hyperinsulinemic hypoglycemia familial 3
|CLNACC=RCV000017520.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1375:C1865290:602485
}}