Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs118204060
LPL
0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 9
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs1800849 0.851 0.160 11 74009120 upstream gene variant G/A;T snv 5
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs372359132 0.827 0.160 5 7878203 missense variant A/G snv 4.0E-06 2.1E-05 5
rs4788102 0.851 0.160 16 28862077 intron variant G/A snv 0.34 6
rs5082 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs6234 0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs663129 0.882 0.160 18 60171168 intergenic variant G/A snv 0.24 4
rs6782181 0.851 0.160 3 138386212 intron variant G/A;C snv 6
rs749710704 0.790 0.160 5 79119289 missense variant C/G;T snv 4.0E-06; 4.0E-06 7
rs7901695 0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs9282541 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs11196205 0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs7211 0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13