Source: GWASCAT

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 3 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: 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 2 2012 2017
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: 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: rs13164856
rs13164856
1.000 0.120 5 132477512 intron variant T/C snv 0.32
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.700 1.000 2 2015 2018
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2016
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 2 2015 2016
dbSNP: rs3749833
rs3749833
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2019 2019
dbSNP: rs1004234
rs1004234
0.827 0.120 5 132421409 intron variant A/G;T snv
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs1004234
rs1004234
0.827 0.120 5 132421409 intron variant A/G;T snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs1004234
rs1004234
0.827 0.120 5 132421409 intron variant A/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs1004234
rs1004234
0.827 0.120 5 132421409 intron variant A/G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs1004234
rs1004234
0.827 0.120 5 132421409 intron variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs10076733
rs10076733
1.000 0.040 5 132425039 intron variant G/T snv 0.17
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.700 1.000 1 2019 2019
dbSNP: rs1012793
rs1012793
5 132445653 intron variant G/A;C snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2017 2017
dbSNP: rs1023518
rs1023518
1.000 0.080 5 132458080 intron variant G/T snv 0.26
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs10900807
rs10900807
5 132421788 intron variant G/C snv 0.20
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
0.700 1.000 1 2019 2019
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
0.700 1.000 1 2015 2015