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.
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 2 2005 2020
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2005 2005
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2005 2005
Glioma
CUI: C0017638
Disease: Glioma
353 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2005 2005
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2005 2005
Refractory cancer
CUI: C0677936
Disease: Refractory cancer
9 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2005 2005
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.050 1.000 5 2006 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.050 0.800 5 2006 2010
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.040 0.750 4 2006 2013
Seizures
CUI: C0036572
Disease: Seizures
553 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.040 0.500 4 2006 2014
Adult Acute Myeloblastic Leukemia
CUI: C0220615
Disease: Adult Acute Myeloblastic Leukemia
3 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 0.500 2 2006 2008
Human immunodeficiency virus (HIV) II infection category B1
56 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2006 2011
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
125 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2006 2012
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2006 2006
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2006 2006
Familial hypercholesterolemia - heterozygous
34 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2006 2006
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
27 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2006 2006
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
308 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2006 2006
Neurobehavioral Manifestations
CUI: C0525041
Disease: Neurobehavioral Manifestations
3 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2006 2006
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2006 2006
Tremor
CUI: C0040822
Disease: Tremor
52 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2006 2006
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.950 20 2007 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.944 18 2007 2017
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
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.040 1.000 4 2007 2015