rs1045642, ABCB1

N. diseases: 214
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.
Drug Resistant Epilepsy
CUI: C1096063
Disease: Drug Resistant Epilepsy
35 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.750 16 2007 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.786 14 2005 2017
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.909 11 2009 2017
Childhood Acute Lymphoblastic Leukemia
261 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.600 10 2003 2017
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.080 0.875 8 2011 2017
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.080 0.875 8 2009 2017
Malignant neoplasm of colon and/or rectum
502 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.060 0.833 6 2008 2017
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.050 1.000 5 2009 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.040 0.750 4 2008 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.040 0.750 4 2008 2017
Infantile nystagmus syndrome
CUI: C1533172
Disease: Infantile nystagmus syndrome
8 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.030 0.667 3 2015 2017
Akathisia
CUI: C0392156
Disease: Akathisia
12 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2010 2017
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2012 2017
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2012 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2016 2017
Idiopathic Nephrotic Syndrome
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
72 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2015 2017
Nephrotic Syndrome, Minimal Change
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
10 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2015 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2017 2017
Gastrointestinal mucositis
CUI: C0521585
Disease: Gastrointestinal mucositis
19 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2017 2017
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2017 2017
Mixed cryoglobulinemia
CUI: C0543697
Disease: Mixed cryoglobulinemia
5 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2017 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.060 0.500 6 2004 2016
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.040 1.000 4 2013 2016
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.030 1.000 3 2010 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2014 2016