Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs220733 1.000 0.080 6 159897771 intron variant A/C;G snv 0.99 3
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs7190256 0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs1492099 0.882 0.120 3 148719716 intron variant T/A;C snv 0.89 5
rs4999127 1.000 0.080 1 154741530 intron variant G/A snv 0.89 1
rs7698692 1.000 0.080 4 173682953 intergenic variant G/A snv 0.88 1
rs2012809 1.000 0.080 5 128854670 intron variant A/G snv 0.86 1
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs2286466 1.000 0.080 16 1964282 synonymous variant A/G snv 0.81 0.86 1
rs6560886 1.000 0.080 12 132573624 intron variant T/C snv 0.86 1
rs6590357 0.882 0.120 11 128911444 synonymous variant T/C snv 0.84 0.85 3
rs2660304 0.925 0.120 1 98046571 non coding transcript exon variant G/T snv 0.83 2
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs244017 1.000 0.080 4 110334761 intergenic variant G/T snv 0.81 1
rs10773657 1.000 0.080 12 122843353 intron variant C/A snv 0.81 1
rs2860482 1.000 0.080 12 56712154 downstream gene variant A/C snv 0.80 1
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs3825214 0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs7508 1.000 0.080 8 18056461 3 prime UTR variant G/A snv 0.77 1
rs4615152 1.000 0.080 4 173678308 intergenic variant T/C snv 0.77 1
rs7529220 1.000 0.080 1 21956126 intron variant T/C snv 0.76 1
rs6462078 1.000 0.080 7 28373568 intron variant C/A snv 0.76 1
rs7961581 0.827 0.200 12 71269322 intron variant C/T snv 0.75 7
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs10163755 0.827 0.200 18 31405413 intron variant G/A snv 0.74 6