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: rs17465637
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.840 1.000 3 2007 2013
dbSNP: rs2133189
rs2133189
MIA3
0.925 0.040 1 222641100 intron variant C/T snv 0.56
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012
dbSNP: rs2291832
rs2291832
MIA3
1.000 0.040 1 222653139 intron variant G/A;C snv 0.64; 1.2E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011