ICAM1, intercellular adhesion molecule 1, 3383

N. diseases: 737; N. variants: 18
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5030359
rs5030359 		19 10277786 intron variant G/A snv 2.1E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs5030359
rs5030359 		19 10277786 intron variant G/A snv 2.1E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs1426809883
rs1426809883 		19 10284797 missense variant G/A snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs199957421
rs199957421 		19 10281703 intron variant -/C delins 7.6E-04
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0.010 1.000 1 2016 2016
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 < 0.001 1 2016 2016
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 < 0.001 1 2016 2016
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0677898
Disease: invasive cancer
invasive cancer 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs281432
rs281432 		0.851 0.280 19 10279982 intron variant C/G snv 0.52
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3093030
rs3093030 		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 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3093030
rs3093030 		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 		0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0677898
Disease: invasive cancer
invasive cancer 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030 		0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0018939
Disease: Hematological Disease
Hematological Disease 		Hemic and Lymphatic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030 		0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030 		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 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs5030339
rs5030339 		19 10269461 intron variant G/A snv 3.4E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5030339
rs5030339 		19 10269461 intron variant G/A snv 3.4E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5030339
rs5030339 		19 10269461 intron variant G/A snv 3.4E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012