rs6922269, MTHFD1L

N. diseases: 7
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 0.807 0.200 6 150931849 intron variant G/A snv 0.35 0.830 1.000 5 2007 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.807 0.200 6 150931849 intron variant G/A snv 0.35 0.040 1.000 4 2010 2015
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.807 0.200 6 150931849 intron variant G/A snv 0.35 0.020 1.000 2 2011 2015
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.807 0.200 6 150931849 intron variant G/A snv 0.35 0.020 1.000 2 2014 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.200 6 150931849 intron variant G/A snv 0.35 0.020 0.500 2 2009 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.200 6 150931849 intron variant G/A snv 0.35 0.020 1.000 2 2009 2014
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.807 0.200 6 150931849 intron variant G/A snv 0.35 0.010 1 2015 2015