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: 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: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0265706
Disease: Gastroschisis
Gastroschisis 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0032533
Disease: Polymyalgia Rheumatica
Polymyalgia Rheumatica 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.010 1.000 1 2000 2000
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C1619727
Disease: Decompensated cirrhosis of liver
Decompensated cirrhosis of liver 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C4699184
Disease: Fuchs
Fuchs 		0.010 1.000 1 2010 2010
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0153633
Disease: Malignant neoplasm of brain
Malignant neoplasm of brain 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis 		Digestive System Diseases 0.010 < 0.001 1 2004 2004
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia 		Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0860564
Disease: Retinoic acid syndrome
Retinoic acid syndrome 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2007 2007
dbSNP: rs1799969
rs1799969 		0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0750974
Disease: Brain Tumor, Primary
Brain Tumor, Primary 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2013 2013