Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Glucose-6-phosphate transport defect
0.800 GeneticVariation UNIPROT Glycogen storage disease type Ib: structural and mutational analysis of the microsomal glucose-6-phosphate transporter gene. 10482875 1999
Glucose-6-phosphate transport defect
0.800 CausalMutation CLINVAR Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b. 10026167 1999
Glucose-6-phosphate transport defect
0.800 GeneticVariation UNIPROT The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a. 10482962 1999
Glucose-6-phosphate transport defect
0.800 GeneticVariation CLINVAR Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b. 10026167 1999
Glucose-6-phosphate transport defect
0.800 GeneticVariation UNIPROT Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11. 9675154 1998
Glucose-6-phosphate transport defect
0.800 GeneticVariation UNIPROT Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib. 9856496 1998
Glucose-6-phosphate transport defect
0.800 GeneticVariation UNIPROT A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic. 9758626 1998
Glucose-6-phosphate transport defect
0.800 GeneticVariation UNIPROT Structure and mutation analysis of the glycogen storage disease type 1b gene. 9781688 1998
Glucose-6-phosphate transport defect
0.800 GeneticVariation UNIPROT Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib. 9428641 1997