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: rs7518199
rs7518199
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs7518199
rs7518199
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011
dbSNP: rs7518199
rs7518199
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs7529229
rs7529229
0.851 0.120 1 154448302 intron variant T/C snv 0.48
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2011 2011
dbSNP: rs7529229
rs7529229
0.851 0.120 1 154448302 intron variant T/C snv 0.48
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011
dbSNP: rs7529229
rs7529229
0.851 0.120 1 154448302 intron variant T/C snv 0.48
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs7529229
rs7529229
0.851 0.120 1 154448302 intron variant T/C snv 0.48
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013