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.
Central nervous system depression (disorder)
CUI: C0151559
Disease: 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
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
Lymphoid leukemia
CUI: C0023448
Disease: Lymphoid leukemia
4 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2014 2014
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
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
Schizophrenia and related disorders
CUI: C0809983
Disease: Schizophrenia and related disorders
5 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2010 2010
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
Myeloid Leukemia
CUI: C0023470
Disease: Myeloid Leukemia
7 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2014 2014
Infantile nystagmus syndrome
CUI: C1533172
Disease: Infantile nystagmus syndrome
8 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.030 0.667 3 2015 2017
Nephrotic Syndrome, Minimal Change
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
10 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.030 1.000 3 2015 2017
Bullous pemphigoid
CUI: C0030805
Disease: Bullous pemphigoid
11 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2017 2018
Nausea and vomiting
CUI: C0027498
Disease: Nausea and vomiting
11 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2014 2014
Akathisia
CUI: C0392156
Disease: Akathisia
12 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2010 2017
Sexual Dysfunction
CUI: C0549622
Disease: Sexual Dysfunction
12 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2013 2013
Dizziness
CUI: C0012833
Disease: Dizziness
14 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2012 2012
Pain, Postoperative
CUI: C0030201
Disease: Pain, Postoperative
14 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2012 2012
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
Sleep Apnea, Central
CUI: C0520680
Disease: Sleep Apnea, Central
17 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2011 2011
Postoperative Nausea and Vomiting
CUI: C0520909
Disease: Postoperative Nausea and Vomiting
18 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2010 2010
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
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
Neoplasm, Residual
CUI: C0242596
Disease: Neoplasm, Residual
23 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2008 2008
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
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
27 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2010 2010
Familial hypercholesterolemia - heterozygous
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
34 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2006 2006