Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5174 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs747760223 0.882 0.120 3 39412034 missense variant T/C snv 4.0E-06 7.0E-06 3
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237