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: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.880 1.000 2 2007 2018
dbSNP: rs17465637
rs17465637
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.840 1.000 1 2008 2012
dbSNP: rs3782886
rs3782886
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.820 1.000 2 2011 2019
dbSNP: rs12526453
rs12526453
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.820 1.000 1 2009 2015
dbSNP: rs9982601
rs9982601
0.851 0.080 21 34226827 intron variant C/T snv 0.15
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.820 1.000 1 2009 2016
dbSNP: rs10738607
rs10738607
0.925 0.080 9 22088095 intron variant A/G snv 0.42
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.810 1.000 1 2007 2018
dbSNP: rs11206510
rs11206510
0.763 0.240 1 55030366 intergenic variant T/A;C;G snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.810 1.000 1 2009 2017
dbSNP: rs1122608
rs1122608
0.763 0.120 19 11052925 intron variant G/T snv 0.18
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.810 0.500 1 2009 2014
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.810 1.000 1 2009 2012
dbSNP: rs11748327
rs11748327
1.000 0.080 5 4029676 downstream gene variant C/T snv 0.21
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.800 1.000 1 2011 2011
dbSNP: rs1746048
rs1746048
0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.800 1.000 1 2009 2009
dbSNP: rs3803915
rs3803915
1.000 0.080 19 2160530 intron variant C/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.800 1.000 1 2015 2015
dbSNP: rs4618210
rs4618210
1.000 0.080 3 17082892 intron variant A/G snv 0.56
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.800 1.000 1 2015 2015
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: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.780 1.000 1 2011 2014
dbSNP: rs2383207
rs2383207
0.695 0.280 9 22115960 intron variant A/G snv 0.64
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.770 1.000 1 2007 2013
dbSNP: rs2569512
rs2569512
0.925 0.080 19 10679486 intron variant T/C snv 0.76
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.740 1.000 1 2011 2011
dbSNP: rs1333045
rs1333045
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.730 1.000 1 2007 2018
dbSNP: rs9925481
rs9925481
0.882 0.160 16 11003622 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.730 1.000 1 2009 2011
dbSNP: rs12373237
rs12373237
0.851 0.200 18 23845972 intron variant G/A snv 0.47
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.720 1.000 1 2010 2011
dbSNP: rs1333040
rs1333040
0.732 0.280 9 22083405 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.720 0.667 1 2007 2011
dbSNP: rs2331291
rs2331291
1.000 0.080 22 26662857 intron variant C/T snv 0.11
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.710 1.000 1 2006 2006
dbSNP: rs10116277
rs10116277
0.827 0.160 9 22081398 intron variant G/T snv 0.62
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2007 2007
dbSNP: rs10263017
rs10263017
1.000 0.080 7 6026173 intron variant G/C;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011