Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs3812316
MLXIPL
0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38 10
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 8