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: rs17114046
rs17114046
PLPP3
0.925 0.040 1 56500678 intron variant A/G snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 2 2011 2011
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: rs2404715
rs2404715
PLPP3
1.000 0.040 1 56543106 intron variant C/T snv 7.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011