Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs223828 0.882 0.240 16 57413502 intron variant T/A;C snv 3
rs663129 0.882 0.160 18 60171168 intergenic variant G/A snv 0.24 4
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
rs372359132 0.827 0.160 5 7878203 missense variant A/G snv 4.0E-06 2.1E-05 5
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs4788102 0.851 0.160 16 28862077 intron variant G/A snv 0.34 6
rs6782181 0.851 0.160 3 138386212 intron variant G/A;C snv 6
rs7211 0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs7901695 0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs11196205 0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs749710704 0.790 0.160 5 79119289 missense variant C/G;T snv 4.0E-06; 4.0E-06 7
rs1467568 0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs2297508 0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05 8
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
rs118204060
LPL
0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 9
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs3737787 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs7566605 0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11