Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs7120118 0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs1042034 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3812316 0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs174601 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs676210 0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs17145738 0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 11
rs6882076 0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs1748195 0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs440446 0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8