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: rs1333048
rs1333048
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs1333048
rs1333048
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2016
dbSNP: rs7341786
rs7341786
9 22112242 intron variant A/C snv 0.65
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs1333048
rs1333048
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2007 2007
dbSNP: rs1333048
rs1333048
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2007 2007
dbSNP: rs7341786
rs7341786
9 22112242 intron variant A/C snv 0.65
Ankle brachial pressure index (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs10757269
rs10757269
1.000 0.040 9 22072265 intron variant A/C;G snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs10757269
rs10757269
1.000 0.040 9 22072265 intron variant A/C;G snv
Ankle brachial pressure index (observable entity)
0.800 1.000 1 2012 2012
dbSNP: rs10757269
rs10757269
1.000 0.040 9 22072265 intron variant A/C;G snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs10757270
rs10757270
1.000 0.040 9 22072720 intron variant A/C;G snv 0.40
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs10757270
rs10757270
1.000 0.040 9 22072720 intron variant A/C;G snv 0.40
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2013 2013
dbSNP: rs2383205
rs2383205
0.925 0.080 9 22060936 intron variant A/C;G snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs2383205
rs2383205
0.925 0.080 9 22060936 intron variant A/C;G snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2013 2013
dbSNP: rs10738609
rs10738609
1.000 0.040 9 22114496 intron variant A/C;G;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs10738609
rs10738609
1.000 0.040 9 22114496 intron variant A/C;G;T snv
Ankle brachial pressure index (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs10738609
rs10738609
1.000 0.040 9 22114496 intron variant A/C;G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs1004638
rs1004638
1.000 0.040 9 22115590 intron variant A/C;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs10738610
rs10738610
0.882 0.120 9 22123767 intron variant A/C;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs1004638
rs1004638
1.000 0.040 9 22115590 intron variant A/C;T snv
Ankle brachial pressure index (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs10738610
rs10738610
0.882 0.120 9 22123767 intron variant A/C;T snv
Ankle brachial pressure index (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs10738610
rs10738610
0.882 0.120 9 22123767 intron variant A/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10811652
rs10811652
0.882 0.120 9 22077086 intron variant A/C;T snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs543830
rs543830
1.000 0.040 9 22026640 intron variant A/C;T snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs543830
rs543830
1.000 0.040 9 22026640 intron variant A/C;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2011 2011
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