rs3024505, None

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.850 0.875 8 2008 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.840 0.889 9 2008 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.810 1.000 3 2012 2017
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.800 1.000 3 2009 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.720 1.000 4 2009 2015
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
52 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.700 1.000 1 2011 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.700 1.000 1 2011 2011
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.040 1.000 4 2012 2015
Anemia
CUI: C0002871
Disease: Anemia
94 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.010 1.000 1 2016 2016
Drug usage
CUI: C0242510
Disease: Drug usage
21 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.010 1.000 1 2013 2013