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.
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO, SOMATIC
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.700 0
Splenomegaly
CUI: C0038002
Disease: Splenomegaly
19 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.700 0
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
Hormone refractory prostate cancer
CUI: C1328504
Disease: Hormone refractory prostate cancer
29 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1 2010 2010
Myelodysplastic-Myeloproliferative Diseases
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1 2013 2013
Myeloid Leukemia
CUI: C0023470
Disease: Myeloid Leukemia
7 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1 2010 2010
Trigeminal Neuralgia
CUI: C0040997
Disease: Trigeminal Neuralgia
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1 2018 2018
Vascular Hemostatic Disorders
CUI: C0600502
Disease: Vascular Hemostatic Disorders
1 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1 2014 2014
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
Lymphoproliferative Disorders
CUI: C0024314
Disease: Lymphoproliferative Disorders
14 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.020 0.500 2 2007 2009
Myelofibrosis due to another disorder
6 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.040 0.750 4 2006 2010
secondary acute myeloid leukemia
CUI: C0280449
Disease: secondary acute myeloid leukemia
8 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.050 0.800 5 2007 2018
Leukocytosis
CUI: C0023518
Disease: Leukocytosis
4 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.100 0.818 11 2006 2017
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
Childhood Myelodysplastic Syndrome
CUI: C2347761
Disease: Childhood 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
Hepatic Vein Thrombosis
CUI: C0019154
Disease: Hepatic Vein Thrombosis
4 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.070 0.857 7 2006 2016
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.100 0.889 18 2008 2019
Budd-Chiari Syndrome
CUI: C0856761
Disease: Budd-Chiari Syndrome
4 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.770 0.900 10 2006 2016
Thrombocytosis
CUI: C0836924
Disease: Thrombocytosis
12 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.100 0.920 25 2006 2018
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.100 0.929 14 2005 2018
Myelofibrosis
CUI: C0026987
Disease: Myelofibrosis
7 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.100 0.944 72 2005 2019
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.900 0.960 274 2005 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.900 0.966 29 2005 2019
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.800 0.966 175 2005 2020