rs1187513719, CYP2C19

N. diseases: 4
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.
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 0.010 1.000 1 2019 2019
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 0.010 1.000 1 2019 2019
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 0.010 1.000 1 2011 2011
Angina, Unstable
CUI: C0002965
Disease: Angina, Unstable
21 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 0.010 1.000 1 2013 2013