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.
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2015 2015
Luminal A Breast Carcinoma
CUI: C3642345
Disease: Luminal A Breast Carcinoma
11 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2015 2015
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2015 2015
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2015 2015
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2014 2014
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
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2014 2015
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2014 2015
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.020 1.000 2 2014 2015
Anemia
CUI: C0002871
Disease: Anemia
94 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Angina Pectoris, Variant
CUI: C0002963
Disease: Angina Pectoris, Variant
4 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2014 2014
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Epilepsies, Partial
CUI: C0014547
Disease: Epilepsies, Partial
23 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Erythema Nodosum
CUI: C0014743
Disease: Erythema Nodosum
3 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2014 2014
Invasive Ductal Breast Carcinoma
CUI: C1134719
Disease: Invasive Ductal Breast Carcinoma
16 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2014 2014
Juvenile Myoclonic Epilepsy
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
46 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Mesial temporal lobe epilepsy with hippocampal sclerosis
7 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Nausea and vomiting
CUI: C0027498
Disease: Nausea and vomiting
11 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Pseudofolliculitis
CUI: C0406191
Disease: Pseudofolliculitis
1 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2014 2014
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1 2014 2014
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
Xeroderma Pigmentosum, Complementation Group D
111 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
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