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
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: 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
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: 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
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
dbSNP: rs5030339
rs5030339
19 10269461 intron variant G/A snv 3.4E-03
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs5030339
rs5030339
19 10269461 intron variant G/A snv 3.4E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs5030359
rs5030359
19 10277786 intron variant G/A snv 2.1E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs5030361
rs5030361
19 10278833 intron variant C/T snv 6.8E-04
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs5030361
rs5030361
19 10278833 intron variant C/T snv 6.8E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs5030361
rs5030361
19 10278833 intron variant C/T snv 6.8E-04
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs5030361
rs5030361
19 10278833 intron variant C/T snv 6.8E-04
High density lipoprotein measurement
0.700 1.000 1 2012 2012