Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2230808 0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
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
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
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
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
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
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
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
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs3846662 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12