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
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
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: 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: C0848771
Disease: neurological disability
neurological disability 		0.010 1.000 1 2017 2017
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: C0940937
Disease: precancerous lesions
precancerous lesions 		0.010 1.000 1 2016 2016
dbSNP: rs3093030
rs3093030 		0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0.010 1.000 1 2016 2016
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
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
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
CUI: C0392885
Disease: High density lipoprotein measurement
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
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
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
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5030383
rs5030383 		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 		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 		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 		0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0848771
Disease: neurological disability
neurological disability 		0.010 1.000 1 2017 2017
dbSNP: rs5498
rs5498 		0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2016 2016
dbSNP: rs5498
rs5498 		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: rs5498
rs5498 		0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2009 2009
dbSNP: rs5498
rs5498 		0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0.010 1.000 1 2016 2016