rs4739066, YTHDF3

N. diseases: 2
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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.080 8 63191534 intron variant A/G snv 0.12 0.710 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.925 0.080 8 63191534 intron variant A/G snv 0.12 0.010 1.000 1 2016 2016