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.
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
64 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.840 0.750 5 2010 2018
Anemia
CUI: C0002871
Disease: Anemia
44 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.800 0.833 13 2010 2018
Inosine Triphosphatase Deficiency
CUI: C0342800
Disease: Inosine Triphosphatase Deficiency
1 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.700 2 2002 2003
response to ribavirin
CUI: C3547186
Disease: response to ribavirin
1 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.700 1 2010 2010
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
89 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.030 1.000 3 2011 2017
Leukopenia
CUI: C0023530
Disease: Leukopenia
63 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.020 0.500 2 2006 2016
Anemia, Hemolytic
CUI: C0002878
Disease: Anemia, Hemolytic
9 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.020 1.000 2 2012 2014
Anemia, severe
CUI: C0238644
Disease: Anemia, severe
1 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.020 1.000 2 2010 2016
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
674 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.020 1.000 2 2009 2010
Influenza-like symptoms
CUI: C0392171
Disease: Influenza-like symptoms
1 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2009 2009
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
48 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2015 2015
Hepatitis A
CUI: C0019159
Disease: Hepatitis A
8 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2017 2017
Febrile Neutropenia
CUI: C0746883
Disease: Febrile Neutropenia
9 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2010 2010
Childhood Acute Lymphoblastic Leukemia
97 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2015 2015
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
215 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2014 2014
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
71 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2015 2015
Hepatitis C Virus Infection
CUI: C4288963
Disease: Hepatitis C Virus Infection
6 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2017 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
451 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2006 2006
Coinfection
CUI: C0275524
Disease: Coinfection
8 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2012 2012
Hepatitis
CUI: C0019158
Disease: Hepatitis
7 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2017 2017
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
99 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 0.010 1.000 1 2010 2010