rs77375493, INSL6;JAK2

N. diseases: 187
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
5q-syndrome
CUI: C0740302
Disease: 5q-syndrome
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2009 2009
Acquired von Willebrand's disease
CUI: C0272362
Disease: Acquired von Willebrand's disease
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2017 2017
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2012 2012
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2009 2009
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2016 2016
Acute Erythroblastic Leukemia
CUI: C0023440
Disease: Acute Erythroblastic Leukemia
5 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.070 1.000 7 2006 2017
Acute erythroleukemia
CUI: C2930974
Disease: Acute erythroleukemia
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2009 2009
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.030 1.000 3 2005 2013
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2010 2010
Acute Megakaryocytic Leukemias
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
15 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.020 1.000 2 2005 2006
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.020 0.500 2 2007 2018
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2017 2017
Adjustment Disorders
CUI: C0001546
Disease: Adjustment Disorders
4 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2009 2009
Adult Erythroleukemia
CUI: C2347748
Disease: Adult Erythroleukemia
4 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.050 1.000 5 2006 2017
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2005 2005
Adult Myelodysplastic Syndrome
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
20 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.060 0.833 6 2006 2018
Anemia
CUI: C0002871
Disease: Anemia
94 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.040 1.000 4 2006 2015
anemia hemoglobin
CUI: C0740992
Disease: anemia hemoglobin
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2015 2015
Arteriopathic disease
CUI: C0852949
Disease: Arteriopathic disease
14 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2019 2019
Autoimmune thrombocytopenia
CUI: C0242584
Disease: Autoimmune thrombocytopenia
7 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2019 2019
B-CELL MALIGNANCY, LOW-GRADE
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
19 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2012 2012
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1 2012 2012
Blast Phase
CUI: C0005699
Disease: Blast Phase
14 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1 2006 2006
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2014 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2019 2019