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: rs2188962
rs2188962
0.882 0.160 5 132435113 intron variant C/T snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 2 2008 2017
dbSNP: rs12521868
rs12521868
1.000 0.040 5 132448701 intron variant G/T snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 1 2010 2012
dbSNP: rs11242111
rs11242111
5 132420366 intron variant A/G;T snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2013 2013
dbSNP: rs2070729
rs2070729
5 132484229 non coding transcript exon variant C/A;T snv 0.52
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2011 2011
dbSNP: rs2106854
rs2106854
5 132433482 intron variant C/T snv 0.23
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2013 2013
dbSNP: rs2188962
rs2188962
0.882 0.160 5 132435113 intron variant C/T snv 0.29
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs2522056
rs2522056
5 132466034 intron variant G/A snv 0.25
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2009 2009
dbSNP: rs11242111
rs11242111
5 132420366 intron variant A/G;T snv
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2013 2013
dbSNP: rs11242111
rs11242111
5 132420366 intron variant A/G;T snv
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2013 2013
dbSNP: rs2106854
rs2106854
5 132433482 intron variant C/T snv 0.23
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2013 2013
dbSNP: rs2106854
rs2106854
5 132433482 intron variant C/T snv 0.23
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2013 2013
dbSNP: rs2188962
rs2188962
0.882 0.160 5 132435113 intron variant C/T snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011
dbSNP: rs2188962
rs2188962
0.882 0.160 5 132435113 intron variant C/T snv 0.29
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2011 2011
dbSNP: rs2248116
rs2248116
1.000 0.040 5 132468655 intron variant C/A snv 0.70
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs2522056
rs2522056
5 132466034 intron variant G/A snv 0.25
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2009 2009
dbSNP: rs2522056
rs2522056
5 132466034 intron variant G/A snv 0.25
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2009 2009
dbSNP: rs2522057
rs2522057
1.000 0.040 5 132466255 intron variant G/A;C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2007 2007
dbSNP: rs4705862
rs4705862
1.000 0.120 5 132477527 intron variant A/T snv 0.51
Oligoarticular Juvenile Idiopathic Arthritis
0.700 1.000 1 2013 2013
dbSNP: rs6873426
rs6873426
5 132482939 3 prime UTR variant G/T snv 0.38
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011
dbSNP: rs6873426
rs6873426
5 132482939 3 prime UTR variant G/T snv 0.38
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2011 2011
dbSNP: rs6873426
rs6873426
5 132482939 3 prime UTR variant G/T snv 0.38
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs6874639
rs6874639
5 132443024 intron variant A/G snv 0.24
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 1 2011 2011
dbSNP: rs6874639
rs6874639
5 132443024 intron variant A/G snv 0.24
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 1 2011 2011
dbSNP: rs6874639
rs6874639
5 132443024 intron variant A/G snv 0.24
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2011 2011