JAK2, Janus kinase 2, 3717

N. diseases: 644; N. variants: 54
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121912473
rs121912473
0.925 0.080 9 5070026 missense variant AA/TT mnv
ERYTHROCYTOSIS, JAK2-RELATED, SOMATIC
0.700 0
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO, SOMATIC
0.700 0
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
Pathological Conditions, Signs and Symptoms 0.700 0
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0036690
Disease: Septicemia
Septicemia
Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2005 2005
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0024299
Disease: Lymphoma
Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0243026
Disease: Sepsis
Sepsis
Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2005 2005
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0027013
Disease: Myeloid Metaplasia
Myeloid Metaplasia
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias
Neoplasms 0.020 1.000 2 2005 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.020 1.000 2 2006 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
Refractory anemia with ringed sideroblasts associated with marked thrombocytosis
Hemic and Lymphatic Diseases 0.010 1.000 1 2006 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2006 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
Myelodysplastic/myeloproliferative neoplasm, unclassifiable
Hemic and Lymphatic Diseases 0.010 1.000 1 2006 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0005699
Disease: Blast Phase
Blast Phase
Pathological Conditions, Signs and Symptoms; Neoplasms; Hemic and Lymphatic Diseases 0.010 < 0.001 1 2006 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C1282609
Disease: Granulocytosis
Granulocytosis
Hemic and Lymphatic Diseases 0.010 1.000 1 2006 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia
Hemic and Lymphatic Diseases 0.010 1.000 1 2006 2006
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
Idiopathic Hypereosinophilic Syndrome
Hemic and Lymphatic Diseases 0.020 1.000 2 2005 2007
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
Extramedullary Hematopoiesis (disorder)
Hemic and Lymphatic Diseases 0.020 1.000 2 2007 2007
dbSNP: rs368927897
rs368927897
0.790 0.240 9 5072541 missense variant G/A;T snv 2.8E-05; 6.4E-05
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease
Hemic and Lymphatic Diseases 0.700 1.000 1 2007 2007
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C1540912
Disease: Hypereosinophilic syndrome
Hypereosinophilic syndrome
Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
Monoclonal Gammopathy of Undetermined Significance
Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0346421
Disease: Chronic eosinophilic leukemia
Chronic eosinophilic leukemia
Neoplasms; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion
Eye Diseases; Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
Disseminated eosinophilic collagen disease
Skin and Connective Tissue Diseases 0.010 1.000 1 2007 2007