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: rs1050152
rs1050152
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 0.917 1 2006 2017
dbSNP: rs12777
rs12777
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2009 2016
dbSNP: rs273909
rs273909
1.000 0.040 5 132331660 intron variant A/G snv 9.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 1.000 1 2013 2018
dbSNP: rs12777
rs12777
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2009 2009
dbSNP: rs12777
rs12777
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2009 2009
dbSNP: rs270607
rs270607
5 132313493 intron variant A/G snv 0.69
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2011 2011
dbSNP: rs270607
rs270607
5 132313493 intron variant A/G snv 0.69
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011
dbSNP: rs270607
rs270607
5 132313493 intron variant A/G snv 0.69
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs272888
rs272888
1.000 0.040 5 132329730 intron variant T/C snv 0.71
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs272889
rs272889
5 132329685 intron variant A/G snv 0.64
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2011 2011
dbSNP: rs272889
rs272889
5 132329685 intron variant A/G snv 0.64
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2011 2011