Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5030383
rs5030383
ICAM1 ; ICAM4
19 10286167 3 prime UTR variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs75407602
rs75407602
ICAM1 ; ICAM4
19 10286554 3 prime UTR variant C/T snv 3.1E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs5490
rs5490
ICAM1 ; LOC105372272
0.925 0.080 19 10271151 5 prime UTR variant A/C snv 1.6E-02 6.7E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2006 2006
dbSNP: rs5490
rs5490
ICAM1 ; LOC105372272
0.925 0.080 19 10271151 5 prime UTR variant A/C snv 1.6E-02 6.7E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2006 2006
dbSNP: rs3093030
rs3093030
ICAM1 ; ICAM4
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2012 2012
dbSNP: rs3093030
rs3093030
ICAM1 ; ICAM4
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030
ICAM1 ; ICAM4
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0677898
Disease: invasive cancer
invasive cancer 		0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030
ICAM1 ; ICAM4
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0018939
Disease: Hematological Disease
Hematological Disease 		0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030
ICAM1 ; ICAM4
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030
ICAM1 ; ICAM4
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2015 2015
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.090 0.778 9 2005 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.090 1.000 9 2009 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.060 0.833 6 2004 2018
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.060 1.000 6 2003 2015
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.060 0.500 6 2006 2018
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.060 1.000 6 2009 2018
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.050 1.000 5 2006 2018
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.050 1.000 5 2003 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.050 0.600 5 2000 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.050 0.600 5 2003 2016
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.040 0.500 4 2003 2016
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.040 0.750 4 2006 2018
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.040 0.750 4 2001 2015
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.030 1.000 3 2001 2016
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.030 1.000 3 2001 2016