Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs2894204 1.000 0.040 6 31269284 intron variant C/A;T snv 1
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 1
rs7637773 1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs4640244 17 21380911 intron variant A/G snv 0.33 1
rs900400 0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs1294410 6 6738519 intron variant T/C snv 0.65 1
rs1294421 1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs12110693 6 121837124 intergenic variant G/A snv 0.23 1
rs987763 6 126960402 intron variant C/A;T snv 1
rs1993709 1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs12440667 1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs2820464 1 219519878 intergenic variant G/A;C snv 1
rs11897119 2 66544868 intron variant T/A;C snv 1
rs12731740 1 207851475 intron variant C/T snv 9.1E-02 1
rs55747707 7 73623036 intron variant G/A snv 0.16 1
rs17213965 16 15788110 intron variant C/T snv 0.24 1
rs7246865 19 17108295 intron variant G/A snv 0.36 1
rs6784615 1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1
rs6486060 11 9003083 intron variant G/A snv 0.55 1
rs17109256 14 79473650 intron variant G/A snv 0.21 1
rs3088050 5 177299634 3 prime UTR variant G/A snv 0.18 1
rs10894604 11 132771851 non coding transcript exon variant T/G snv 0.26 1