rs1060499616
RUNX1;LOC112267915
Platelet Disorder, Familial, with Associated Myeloid Malignancy
0.800
GeneticVariation
UNIPROT
rs1060502579
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
G
0.700
GeneticVariation
CLINVAR
rs1555889984
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Hypercellular bone marrow
A
0.700
GeneticVariation
CLINVAR
rs1555889984
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Fatigue
A
0.700
GeneticVariation
CLINVAR
rs1555889984
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Pancytopenia
A
0.700
GeneticVariation
CLINVAR
rs1555889984
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
A
0.700
GeneticVariation
CLINVAR
rs1555889984
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Fever
A
0.700
GeneticVariation
CLINVAR
rs1555899813
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
TCC
0.700
CausalMutation
CLINVAR
rs1569061762
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Thrombocytopenia
T
0.700
GeneticVariation
CLINVAR
rs1569061768
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Thrombocytopenia
A
0.700
GeneticVariation
CLINVAR
rs1569084116
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
G
0.700
GeneticVariation
CLINVAR
rs1569084530
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
GCGCCGGCGTCCGGGGCGCCCAGCGGCAA
0.700
CausalMutation
CLINVAR
rs267607026
RUNX1;LOC112267915
Platelet Disorder, Familial, with Associated Myeloid Malignancy
T
0.700
CausalMutation
CLINVAR
rs587776809
RUNX1;LOC112267915
Platelet Disorder, Familial, with Associated Myeloid Malignancy
A
0.700
CausalMutation
CLINVAR
rs1060499616
RUNX1;LOC112267915
Platelet Disorder, Familial, with Associated Myeloid Malignancy
T
0.800
CausalMutation
CLINVAR
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
10508512
1999
rs1060499616
RUNX1;LOC112267915
Platelet Disorder, Familial, with Associated Myeloid Malignancy
T
0.800
GeneticVariation
CLINVAR
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
10508512
1999
rs74315450
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
0.800
GeneticVariation
UNIPROT
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
10508512
1999
rs74315450
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
T
0.800
CausalMutation
CLINVAR
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
10508512
1999
rs1057519748
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Leukemia, Myelocytic, Acute
A
0.700
GeneticVariation
CLINVAR
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
10508512
1999
rs1057519748
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
A
0.700
CausalMutation
CLINVAR
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
10508512
1999
rs1569061768
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
A
0.700
CausalMutation
CLINVAR
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
10508512
1999
rs1060499616
RUNX1;LOC112267915
Platelet Disorder, Familial, with Associated Myeloid Malignancy
T
0.800
CausalMutation
CLINVAR
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
11830488
2002
rs74315450
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
T
0.800
CausalMutation
CLINVAR
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
11830488
2002
rs121912498
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
C
0.700
CausalMutation
CLINVAR
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
11830488
2002
rs121912499
×
Entrez Id:
861
Gene Symbol:
RUNX1
RUNX1
Platelet Disorder, Familial, with Associated Myeloid Malignancy
T
0.700
CausalMutation
CLINVAR
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
11830488
2002