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: 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: 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
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.020 0.500 2 2011 2016
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		0.020 1.000 2 2000 2016
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.020 < 0.001 2 2007 2013
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.020 1.000 2 2006 2008
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome 		0.020 1.000 2 2017 2019
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.020 1.000 2 2006 2006
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2006 2009
dbSNP: rs5030359
rs5030359
ICAM1
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
ICAM1
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: rs5491
rs5491
ICAM1
0.827 0.160 19 10274864 missense variant A/G;T snv 4.0E-06; 2.8E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.020 1.000 2 2006 2014
dbSNP: rs1426809883
rs1426809883
ICAM1
19 10284797 missense variant G/A snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2006 2006
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0265706
Disease: Gastroschisis
Gastroschisis 		0.010 1.000 1 2006 2006
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2017 2017
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0032533
Disease: Polymyalgia Rheumatica
Polymyalgia Rheumatica 		0.010 1.000 1 2000 2000
dbSNP: rs1799969
rs1799969
ICAM1
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 		0.010 1.000 1 2008 2008
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia 		0.010 1.000 1 2008 2008
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 1.000 1 2006 2006
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 < 0.001 1 2015 2015
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2007 2007
dbSNP: rs1799969
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2013 2013
dbSNP: rs1799969
rs1799969
ICAM1
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