rs1057524900, GCK

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Monogenic diabetes
CUI: C3888631
Disease: Monogenic diabetes
0.700 GeneticVariation CLINVAR Doubling the referral rate of monogenic diabetes through a nationwide information campaign--update on glucokinase gene mutations in a Polish cohort. 22035297 2012
Monogenic diabetes
CUI: C3888631
Disease: Monogenic diabetes
0.700 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
Monogenic diabetes
CUI: C3888631
Disease: Monogenic diabetes
0.700 GeneticVariation CLINVAR Six novel mutations in the GCK gene in MODY patients. 17204055 2007
Monogenic diabetes
CUI: C3888631
Disease: Monogenic diabetes
0.700 GeneticVariation CLINVAR Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents. 16602010 2006
Monogenic diabetes
CUI: C3888631
Disease: Monogenic diabetes
0.700 GeneticVariation CLINVAR Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY). 14517956 2003