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: 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: rs199957421
rs199957421
ICAM1
19 10281703 intron variant -/C delins 7.6E-04
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs5030339
rs5030339
ICAM1 ; LOC105372272
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
ICAM1 ; LOC105372272
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
ICAM1 ; LOC105372272
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
ICAM1 ; LOC105372272
19 10269461 intron variant G/A snv 3.4E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5030339
rs5030339
ICAM1 ; LOC105372272
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
ICAM1
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
ICAM1
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
ICAM1
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
ICAM1
19 10278833 intron variant C/T snv 6.8E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5030361
rs5030361
ICAM1
19 10278833 intron variant C/T snv 6.8E-04
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5030383
rs5030383
ICAM1 ; ICAM4
19 10286167 3 prime UTR variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5030397
rs5030397
ICAM1
19 10281711 intron variant G/A;C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs75407602
rs75407602
ICAM1 ; ICAM4
19 10286554 3 prime UTR variant C/T snv 3.1E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs5491
rs5491
ICAM1
0.827 0.160 19 10274864 missense variant A/G;T snv 4.0E-06; 2.8E-02
CUI: C1855457
Disease: MALARIA, CEREBRAL, SUSCEPTIBILITY TO (finding)
MALARIA, CEREBRAL, SUSCEPTIBILITY TO (finding) 		0.700 0
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.090 0.778 9 2005 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.090 1.000 9 2009 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.060 0.833 6 2004 2018
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.060 1.000 6 2003 2015
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.060 0.500 6 2006 2018
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.060 1.000 6 2009 2018