rs104894816, GATA1

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
0.700 CausalMutation CLINVAR Platelet pathology in sex-linked GATA-1 dyserythropoietic macrothrombocytopenia II. Cytochemistry. 17763153 2007
THROMBOCYTOPENIA, X-LINKED, WITHOUT DYSERYTHROPOIETIC ANEMIA
0.700 CausalMutation CLINVAR
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
0.700 CausalMutation CLINVAR Platelet pathology in carriers of the X-linked GATA-1 macrothrombocytopenia. 18041654 2007
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
0.700 CausalMutation CLINVAR Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation. 11418466 2001
THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA
0.700 GeneticVariation UNIPROT Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation. 11809723 2002
THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA
0.700 GeneticVariation UNIPROT X-linked thrombocytopenia caused by a novel mutation of GATA-1. 11675338 2001
THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA
0.700 GeneticVariation UNIPROT Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1. 10700180 2000
THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA
0.700 GeneticVariation UNIPROT Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation. 11418466 2001
Anemia
CUI: C0002871
Disease: Anemia
0.010 GeneticVariation BEFREE Missense mutations in the N-terminal zinc finger (Nf) of GATA1 result in abnormal hematopoiesis, as documented in four families: the mutation V205M leads to both severe macrothrombocytopenia and dyserythropoietic anemia, D218G to macrothrombocytopenia and mild dyserythropoiesis without anemia, G208S to macrothrombocytopenia and R216Q to macrothrombocytopenia with beta-thalassemia. 11809723 2002
Macrothrombocytopenia
CUI: C2751260
Disease: Macrothrombocytopenia
0.010 GeneticVariation BEFREE Missense mutations in the N-terminal zinc finger (Nf) of GATA1 result in abnormal hematopoiesis, as documented in four families: the mutation V205M leads to both severe macrothrombocytopenia and dyserythropoietic anemia, D218G to macrothrombocytopenia and mild dyserythropoiesis without anemia, G208S to macrothrombocytopenia and R216Q to macrothrombocytopenia with beta-thalassemia. 11809723 2002