Source: GWASCAT

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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2018 2018
dbSNP: rs147055617
rs147055617
PLPP3
1.000 0.040 1 56520631 intron variant A/G snv 8.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs17416285
rs17416285
PLPP3
1.000 0.040 1 56554977 intron variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs4634932
rs4634932
PLPP3
1.000 0.040 1 56530519 intron variant T/C snv 7.2E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs56170783
rs56170783
PLPP3
1.000 0.040 1 56550459 intron variant A/C snv 6.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2017 2017
dbSNP: rs9970807
rs9970807
PLPP3
0.925 0.080 1 56499992 intron variant C/T snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2015 2015