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: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 9 2007 2020
dbSNP: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.900 0.944 2 2007 2019
dbSNP: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.800 1.000 2 2011 2013
dbSNP: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013
dbSNP: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2013 2013
dbSNP: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011