rs5498, ICAM4;ICAM1

N. diseases: 99
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 2 2007 2013
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2015 2015
Biliary Atresia
CUI: C0005411
Disease: Biliary Atresia
32 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2005 2005
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2013 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2015 2015
Chronic thromboembolic pulmonary hypertension
4 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2019 2019
Congenital atresia of extrahepatic bile duct
19 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2005 2005
Icterus
CUI: C0022346
Disease: Icterus
17 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2005 2005
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2013 2013
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1 2004 2004
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.030 0.333 3 2003 2018
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.060 0.500 6 2006 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2003 2003
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2013 2015
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2003 2005
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.020 0.500 2 2001 2015
Diabetes Mellitus, Insulin-Dependent
954 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.050 0.600 5 2000 2019
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.050 0.600 5 2003 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.040 0.750 4 2001 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.040 0.750 4 2006 2018
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.090 0.778 9 2005 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.060 0.833 6 2004 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.090 1.000 9 2009 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.060 1.000 6 2009 2018
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.060 1.000 6 2003 2015