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: 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: 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: 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: 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: 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: 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: rs1638021
rs1638021
1.000 0.080 7 157645345 intron variant T/C;G snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs16980013
rs16980013
1.000 0.080 19 45764195 3 prime UTR variant G/T snv 0.24
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs17038082
rs17038082
1.000 0.080 3 13358775 intron variant G/A snv 3.4E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs17381591
rs17381591
1.000 0.080 10 17202049 non coding transcript exon variant T/C snv 0.28
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs17828052
rs17828052
1.000 0.080 4 7484048 intron variant C/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs178293
rs178293
1.000 0.080 22 20995290 non coding transcript exon variant C/T snv 0.11
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs1794429
rs1794429
1.000 0.080 4 3531339 intron variant C/T snv 0.68
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs1998055
rs1998055
1.000 0.080 14 23154618 intron variant G/A;C snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs2003334
rs2003334
1.000 0.080 3 126103160 upstream gene variant C/T snv 0.36
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs2011973
rs2011973
1.000 0.080 12 3224412 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs2073746
rs2073746
1.000 0.080 22 19991035 intron variant T/C snv 0.80
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs2075624
rs2075624
IVD
1.000 0.080 15 40418524 3 prime UTR variant G/A snv 0.24
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs2123731
rs2123731
1.000 0.080 19 4929461 missense variant A/C;G snv 8.1E-06; 0.30
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs2236030
rs2236030
1.000 0.080 22 50460881 intron variant G/A snv 6.8E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs2236052
rs2236052
1.000 0.080 4 3316686 synonymous variant A/G snv 0.64 0.70
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011