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: rs17465637
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.750 1.000 1 2011 2019
dbSNP: rs67180937
rs67180937
MIA3
1.000 0.040 1 222650401 intron variant T/C;G snv 0.64
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2015 2017
dbSNP: rs17465982
rs17465982
MIA3
1.000 0.040 1 222664597 intron variant G/A snv 0.57
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs2133189
rs2133189
MIA3
0.925 0.040 1 222641100 intron variant C/T snv 0.56
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs35158675
rs35158675
MIA3
1.000 0.040 1 222656208 intron variant G/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018