Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs11234027 0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7944926 0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs884164 0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs544456198 0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187