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: rs6725887
rs6725887
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2014
dbSNP: rs6725887
rs6725887
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.800 1.000 1 2009 2009
dbSNP: rs11691351
rs11691351
2 203009189 intron variant A/G snv 0.42
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs17406900
rs17406900
2 202919479 intron variant A/G snv 0.42
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs3731695
rs3731695
2 202955552 intron variant T/C snv 0.46
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs3845802
rs3845802
2 202875949 3 prime UTR variant T/G snv 0.42
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs3933629
rs3933629
2 202901644 intron variant T/C snv 0.39
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs6725887
rs6725887
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013
dbSNP: rs6725887
rs6725887
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2014 2014