Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs3812316
MLXIPL
0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26