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: rs1539019
rs1539019
0.882 0.240 1 247436999 intron variant A/C snv 0.63
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 2 2009 2011
dbSNP: rs10157379
rs10157379
1 247442297 intron variant C/G;T snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2013 2016
dbSNP: rs12239046
rs12239046
1 247438293 intron variant T/C snv 0.58
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2011 2017
dbSNP: rs12239046
rs12239046
1 247438293 intron variant T/C snv 0.58
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 1 2011 2019
dbSNP: rs1539019
rs1539019
0.882 0.240 1 247436999 intron variant A/C snv 0.63
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 2 2009 2011
dbSNP: rs1539019
rs1539019
0.882 0.240 1 247436999 intron variant A/C snv 0.63
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 2 2009 2011
dbSNP: rs10157379
rs10157379
1 247442297 intron variant C/G;T snv
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2013 2013
dbSNP: rs10157379
rs10157379
1 247442297 intron variant C/G;T snv
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2013 2013
dbSNP: rs12239046
rs12239046
1 247438293 intron variant T/C snv 0.58
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011
dbSNP: rs12239046
rs12239046
1 247438293 intron variant T/C snv 0.58
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs4925659
rs4925659
1 247440161 intron variant G/A snv 0.33
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2011 2011
dbSNP: rs4925659
rs4925659
1 247440161 intron variant G/A snv 0.33
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs4925659
rs4925659
1 247440161 intron variant G/A snv 0.33
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011