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.
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
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: 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
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
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
leukemia
CUI: C0023418
Disease: leukemia
144 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2007 2007
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2009 2009
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2010 2010
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1 2007 2007
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.030 0.333 3 2007 2019
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
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.040 0.750 4 2010 2019
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.040 0.750 4 2014 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.080 0.875 8 2005 2017
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.080 0.875 8 2007 2018
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.080 0.875 8 2005 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.070 1.000 7 2008 2013
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.050 1.000 5 2007 2017
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.050 1.000 5 2007 2017
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.040 1.000 4 2013 2016
Drug Resistant Epilepsy
CUI: C1096063
Disease: Drug Resistant Epilepsy
35 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.040 1.000 4 2008 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.040 1.000 4 2006 2013