Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17114036
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2014
dbSNP: rs17114036
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 2 2013 2018
dbSNP: rs17114036
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0.700 1.000 1 2013 2013