Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10211025 1.000 0.080 2 41801493 intergenic variant A/G snv 0.12 1
rs10508372 1.000 0.080 10 8930055 intergenic variant G/A snv 0.14 1
rs10800812 1.000 0.080 1 202086810 intergenic variant A/G snv 0.77 1
rs10924993 0.925 0.080 1 236296485 intergenic variant T/A;G snv 1
rs10957979 1.000 0.080 8 80377552 intron variant A/G snv 0.61 1
rs11048311 1.000 0.080 12 25869205 downstream gene variant A/C snv 0.18 1
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 1
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 1
rs1229598 1.000 0.080 18 56267556 regulatory region variant A/C;G;T snv 1
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 1
rs12543811 1.000 0.080 8 80366650 intron variant G/A snv 0.62 1
rs1412426 1.000 0.080 9 6188652 intergenic variant A/C;T snv 1
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 1
rs1538084 1.000 0.080 1 152523536 intergenic variant A/C snv 0.79 1
rs1612986 0.925 0.080 10 9022753 intergenic variant T/C snv 0.24 1
rs1663687 1.000 0.080 10 9012824 intergenic variant G/A snv 0.35 1
rs16929496 1.000 0.080 12 25840870 regulatory region variant T/C snv 0.19 1
rs17572584 1.000 0.080 3 143169201 intergenic variant C/T snv 0.11 1
rs2153101 1.000 0.080 1 203199346 intergenic variant A/T snv 0.84 1
rs2425656 1.000 0.080 20 44877606 intron variant G/A snv 0.32 1
rs2538026 1.000 0.080 18 56261410 intergenic variant A/C;G snv 1
rs2589561 1.000 0.080 10 9004682 intergenic variant A/G snv 0.83 1
rs340908 1.000 0.080 9 6128897 intergenic variant T/A;C snv 1
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 1
rs4065985 1.000 0.080 17 39945679 downstream gene variant G/C snv 0.63 1