Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs419598 0.742 0.280 2 113129630 synonymous variant T/C snv 0.26 0.21 13
rs6903608 0.742 0.400 6 32460508 intron variant C/G;T snv 11
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2734986 0.827 0.160 6 29850791 intron variant T/C snv 0.10 5
rs27524 0.851 0.160 5 96766240 intron variant A/G snv 0.61 4
rs6904029 0.851 0.200 6 29975290 non coding transcript exon variant G/A snv 0.29 0.26 4
rs223828 0.882 0.240 16 57413502 intron variant T/A;C snv 3
rs10813831 0.925 0.120 9 32526148 missense variant G/A snv 0.21 0.24 2
rs6457715 0.925 0.120 6 33115411 intron variant A/G snv 0.35 2