Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
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
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44