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.
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
129 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2009 2013
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 0.500 2 2010 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2006 2019
Nephrotic Syndrome
CUI: C0027726
Disease: Nephrotic Syndrome
45 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2011 2013
Pain
CUI: C0030193
Disease: Pain
196 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2010 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2004 2015
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2006 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 1.000 2 2006 2010
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.020 2 2007 2008
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