rs17114036, PLPP3

N. diseases: 5
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 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.800 1.000 2 2011 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.710 1.000 3 2013 2018
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.700 1.000 1 2014 2014
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.700 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.010 1.000 1 2018 2018