Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs2228671 0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs121908029 0.763 0.200 19 11105588 stop gained G/A;C;T snv 1.6E-05; 1.6E-05; 8.1E-06 13
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs3846662 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12