rs2032582, ABCB1

N. diseases: 97
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.
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2016 2016
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2014 2014
Agnosia for Pain
CUI: C0563625
Disease: Agnosia for Pain
25 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2018 2018
Anemia
CUI: C0002871
Disease: Anemia
94 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2014 2014
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2017 2017
Avascular Necrosis of Femur Head
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
20 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2007 2007
Balkan Nephropathy
CUI: C0004698
Disease: Balkan Nephropathy
4 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2004 2004
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2012 2012
Central nervous system depression (disorder)
1 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2013 2013
Childhood Acute Lymphoblastic Leukemia
261 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2007 2007
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2014 2014
Childhood nephrotic syndrome
CUI: C3874381
Disease: Childhood nephrotic syndrome
6 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2011 2011
Cockayne Syndrome, Type I
CUI: C0751039
Disease: Cockayne Syndrome, Type I
42 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2011 2011
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2009 2009
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2008 2008
Complex partial seizures
CUI: C0149958
Disease: Complex partial seizures
5 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2013 2013
Complicated malaria
CUI: C2747816
Disease: Complicated malaria
38 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2013 2013
CYP2D6 polymorphism
CUI: C3203671
Disease: CYP2D6 polymorphism
5 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2015 2015
Delusions
CUI: C0011253
Disease: Delusions
15 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2014 2014
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2018 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2018 2018