rs10159239, NLRP3

N. diseases: 3
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 Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.882 0.040 1 247443750 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.040 1 247443750 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.040 1 247443750 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020