Source: GWASDB

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 2 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 1 2011 2018
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 2 2008 2019
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 2 2011 2019
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 2 2011 2013
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: 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: 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: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 2 2009 2013
dbSNP: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 2 2009 2013
dbSNP: rs2228145
rs2228145
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 2 2009 2013
dbSNP: rs4129267
rs4129267
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 2 2011 2013
dbSNP: rs4129267
rs4129267
0.807 0.200 1 154453788 intron variant C/G;T snv
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 2 2011 2013
dbSNP: rs12089132
rs12089132
1 154405860 intron variant T/C snv 1.2E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12089132
rs12089132
1 154405860 intron variant T/C snv 1.2E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1552481
rs1552481
1 154403877 non coding transcript exon variant C/T snv 0.94
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1552481
rs1552481
1 154403877 non coding transcript exon variant C/T snv 0.94
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs28638007
rs28638007
1 154448878 intron variant T/C snv 9.3E-02
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs4537545
rs4537545
0.790 0.160 1 154446403 intron variant C/T snv 0.48
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs4537545
rs4537545
0.790 0.160 1 154446403 intron variant C/T snv 0.48
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2011 2011
dbSNP: rs4537545
rs4537545
0.790 0.160 1 154446403 intron variant C/T snv 0.48
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011
dbSNP: rs4845618
rs4845618
0.851 0.160 1 154427539 intron variant G/T snv 0.53
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs4845625
rs4845625
0.851 0.080 1 154449591 intron variant T/C snv 0.60
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs4845625
rs4845625
0.851 0.080 1 154449591 intron variant T/C snv 0.60
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013
dbSNP: rs7518199
rs7518199
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2011 2011