rs17465637, MIA3

N. diseases: 11
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.840 1.000 7 2007 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.750 1.000 6 2011 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.840 1.000 5 2008 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.030 1.000 3 2011 2013
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.020 1.000 2 2012 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 1 2012 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 1 2012 2012
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 1 2012 2012
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
45 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 1.000 1 2008 2008
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 1 2012 2012