Source: GWASCAT

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: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.850 0.889 3 2010 2019
dbSNP: rs4129267
rs4129267
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.820 0.667 2 2011 2018
dbSNP: rs4129267
rs4129267
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 3 2011 2019
dbSNP: rs4537545
rs4537545
0.790 0.160 1 154446403 intron variant C/T snv 0.48
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2009 2019
dbSNP: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 1 2008 2019
dbSNP: rs2229238
rs2229238
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2012 2012
dbSNP: rs4129267
rs4129267
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2011 2013
dbSNP: rs4845625
rs4845625
0.851 0.080 1 154449591 intron variant T/C snv 0.60
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 1.000 1 2013 2018
dbSNP: rs8192284
rs8192284
0.724 0.720 1 154454494 missense variant A/C;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.730 1.000 1 2010 2012
dbSNP: rs4129267
rs4129267
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.710 1.000 2 2013 2018
dbSNP: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.710 1.000 1 2013 2015
dbSNP: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C0013595
Disease: Eczema
Eczema
0.710 1.000 1 2013 2019
dbSNP: rs61812598
rs61812598
1.000 0.080 1 154447611 intron variant G/A snv 0.31
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 2 2016 2017
dbSNP: rs6689306
rs6689306
0.925 0.080 1 154423470 intron variant A/G snv 0.61
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 2 2015 2017
dbSNP: rs8192284
rs8192284
0.724 0.720 1 154454494 missense variant A/C;T snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 2 2009 2017
dbSNP: rs12083537
rs12083537
0.882 0.200 1 154408627 intron variant A/G snv 0.22
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs12118721
rs12118721
1.000 0.080 1 154424940 intron variant T/C snv 0.51
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2015 2015
dbSNP: rs12129500
rs12129500
1.000 0.080 1 154451288 intron variant T/C snv 0.60
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2018 2018
dbSNP: rs12133641
rs12133641
0.925 0.040 1 154455807 intron variant A/G snv 0.44
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs12133641
rs12133641
0.925 0.040 1 154455807 intron variant A/G snv 0.44
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
0.700 1.000 1 2017 2017
dbSNP: rs12133641
rs12133641
0.925 0.040 1 154455807 intron variant A/G snv 0.44
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs12730935
rs12730935
1 154447416 intron variant G/A snv 0.27
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs146402667
rs146402667
1 154426077 intron variant CACACACACACACACA/-;CA;CACA;CACACA;CACACACA;CACACACACA;CACACACACACA;CACACACACACACA;CACACACACACACACACA;CACACACACACACACACACA;CACACACACACACACACACACA;CACACACACACACACACACACACA;CACACACACACACACACACACACACA;CACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACA delins 0.39
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019