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: 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: 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: 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
dbSNP: rs10281500
rs10281500
1.000 0.080 7 55475197 intron variant C/G snv 0.32
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs1045274
rs1045274
1.000 0.080 16 580902 synonymous variant C/G;T snv 0.16; 2.0E-05
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
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: 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: rs10811650
rs10811650
0.882 0.200 9 22067594 intron variant A/G snv 0.37
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2007 2007
dbSNP: rs10838532
rs10838532
1.000 0.080 11 45925913 intron variant G/C snv 0.18
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs10986769
rs10986769
0.925 0.120 9 125460061 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
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: 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: rs12027041
rs12027041
1.000 0.080 1 3674884 intron variant G/C snv 0.38
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 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: 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: rs12679196
rs12679196
0.925 0.120 8 139800104 intron variant C/T snv 0.13
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs13051704
rs13051704
1.000 0.080 21 42366262 intron variant G/C snv 8.0E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs1324694
rs1324694
0.925 0.120 10 100186688 upstream gene variant C/T snv 7.8E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs13301354
rs13301354
1.000 0.080 9 137030185 3 prime UTR variant T/C snv 0.64
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 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: 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: rs1333046
rs1333046
0.925 0.080 9 22124124 intron variant T/A snv 0.43
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: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2007 2007