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: rs10757278
rs10757278
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.900 0.923 1 2007 2019
dbSNP: rs10757278
rs10757278
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 3 2008 2016
dbSNP: rs10757278
rs10757278
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 3 2011 2013
dbSNP: rs10757278
rs10757278
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2013 2013