Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2575876 9 104903458 intron variant G/A snv 0.24 7
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs55791371 0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs17249141 19 11089332 upstream gene variant C/T snv 3.3E-03 4
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs11075253 16 15054789 intron variant C/A snv 0.22 1
rs11644601 16 15078261 intron variant T/C snv 0.21 4
rs67418890 1 161571067 intron variant T/A;C snv 1
rs190121281 19 19141970 upstream gene variant G/A snv 3.5E-03 1
rs331
LPL
8 19962894 intron variant G/A snv 0.30 4
rs1059611
LPL
8 19967052 3 prime UTR variant T/C snv 0.13 3
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs676210 0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs12713956 2 21018633 intron variant A/G snv 0.14 4
rs1367117 1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs312985 2 21155933 regulatory region variant A/G snv 0.75 2
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs6917603 6 30049294 intron variant T/C snv 0.15 2
rs4299376 0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs4245791 0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8