Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs777870079
rs777870079
GCK
A 0.810 GeneticVariation CLINVAR

dbSNP: rs193922264
rs193922264
GCK
T 0.800 GeneticVariation CLINVAR Lower Circulating miR-122 Level in Patients with HNF1A Variant-Induced Diabetes Compared with Type 2 Diabetes. 30155490

2018

dbSNP: rs193922264
rs193922264
GCK
T 0.800 GeneticVariation CLINVAR Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia. 24430320

2014

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus. 22060211

2012

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Incidental mild hyperglycemia in children: two MODY 2 families identified in Brazilian subjects. 23295292

2012

dbSNP: rs148311934
rs148311934
T 0.800 GeneticVariation CLINVAR Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations. 20337973

2010

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia. 19790256

2009

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Mild fasting hyperglycemia in children: high rate of glucokinase mutations and some risk of developing type 1 diabetes mellitus. 19309449

2009

dbSNP: rs148311934
rs148311934
T 0.800 GeneticVariation CLINVAR Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia. 19790256

2009

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry. 18399931

2008

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Long-term follow-up of oral glucose tolerance test-derived glucose tolerance and insulin secretion and insulin sensitivity indexes in subjects with glucokinase mutations (MODY2). 18411240

2008

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Glucokinase gene mutations: structural and genotype-phenotype analyses in MODY children from South Italy. 18382660

2008

dbSNP: rs193922264
rs193922264
GCK
T 0.800 GeneticVariation CLINVAR Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain. 17573900

2007

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Genetic and clinical characteristics of Korean maturity-onset diabetes of the young (MODY) patients. 16632067

2006

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Glucokinase mutations in young children with hyperglycemia. 16444761

2006

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients. 16965331

2006

dbSNP: rs148311934
rs148311934
T 0.800 GeneticVariation CLINVAR Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients. 16965331

2006

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI. 11508276

2001

dbSNP: rs1085307455
rs1085307455
A 0.800 CausalMutation CLINVAR A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria. 10753050

2000

dbSNP: rs148311934
rs148311934
T 0.800 GeneticVariation CLINVAR Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families. 9049484

1997

dbSNP: rs104894005
rs104894005
A 0.800 CausalMutation CLINVAR

dbSNP: rs104894008
rs104894008
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894009
rs104894009
G 0.800 CausalMutation CLINVAR

dbSNP: rs104894010
rs104894010
GCK
G 0.800 CausalMutation CLINVAR

dbSNP: rs104894016
rs104894016
GCK
T 0.800 CausalMutation CLINVAR