rs1799969, ICAM1

N. diseases: 38
Source: BEFREE ×
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.
Endometriosis
CUI: C0014175
Disease: Endometriosis
207 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.040 0.500 4 2003 2016
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
202 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.030 1.000 3 2001 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.030 1.000 3 2001 2016
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
76 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.020 1.000 2 2006 2008
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.020 1.000 2 2006 2009
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.020 1.000 2 2000 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
252 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.020 2 2007 2013
Guillain-Barre Syndrome
CUI: C0018378
Disease: Guillain-Barre Syndrome
13 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.020 1.000 2 2017 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
277 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.020 1.000 2 2006 2006
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
307 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.020 0.500 2 2011 2016
Acute Promyelocytic Leukemia
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
21 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2007 2007
Biliary Atresia
CUI: C0005411
Disease: Biliary Atresia
19 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2008 2008
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
85 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2013 2013
Brain Tumor, Primary
CUI: C0750974
Disease: Brain Tumor, Primary
8 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2013 2013
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2007 2007
Congenital atresia of extrahepatic bile duct
CUI: C4520983
Disease: Congenital atresia of extrahepatic bile duct
19 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2008 2008
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
456 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1 2015 2015
Decompensated cirrhosis of liver
CUI: C1619727
Disease: Decompensated cirrhosis of liver
2 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2008 2008
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
1598 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2006 2006
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
159 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2006 2006
Fuchs
CUI: C4699184
Disease: Fuchs
5 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2010 2010
Gastroschisis
CUI: C0265706
Disease: Gastroschisis
8 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2006 2006
Glioma
CUI: C0017638
Disease: Glioma
283 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2013 2013
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
115 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2012 2012
Malignant neoplasm of brain
CUI: C0153633
Disease: Malignant neoplasm of brain
12 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2013 2013