Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.100 0.923 13 2006 2019
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.090 1.000 9 2012 2019
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.060 0.833 6 2011 2019
dbSNP: rs822395
rs822395
0.776 0.240 3 186849018 intron variant C/A;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.030 1.000 3 2012 2019
dbSNP: rs17300539
rs17300539
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs182052
rs182052
0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs185847354
rs185847354
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2004 2004