Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10175368 0.925 0.080 2 38080719 intron variant C/T snv 0.23 4
rs10505346 0.925 0.080 8 118951604 intron variant G/T snv 0.22 4
rs13385191 0.925 0.080 2 20688505 intron variant A/G snv 0.20 4
rs17036508 0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02 4
rs188140481 0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv 4
rs1983891 0.925 0.080 6 41568689 intron variant C/T snv 0.35 4
rs198977 0.925 0.080 19 50878521 missense variant C/T snv 0.24 0.30 4
rs266882 0.925 0.080 19 50854757 upstream gene variant G/A snv 0.49 4
rs2705897 0.925 0.080 4 184631944 splice region variant T/G snv 0.64 0.73 4
rs367590266 0.925 0.080 6 52797630 missense variant T/C snv 1.2E-05 7.0E-06 4
rs368952331 0.925 0.080 15 74722805 missense variant C/T snv 2.8E-05 6.3E-05 4
rs4647603 0.925 0.080 4 184648576 5 prime UTR variant C/T snv 0.11 4
rs6983269 0.925 0.080 8 2741967 intron variant C/A;G;T snv 0.42 4
rs775220785 0.925 0.080 7 99772615 missense variant C/T snv 8.0E-06 4
rs780354238 0.925 0.080 8 42369855 missense variant A/G snv 4.4E-06 4
rs1034528 0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs12653946 0.882 0.080 5 1895715 intron variant C/T snv 0.43 5
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs4919743 0.925 0.080 12 52915800 intron variant G/A snv 0.13 5
rs6504074 0.882 0.120 17 61822429 intron variant G/A;T snv 5
rs7008482 0.882 0.120 8 125255388 intron variant T/G snv 0.48 5
rs7254617 0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv 5
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 6
rs1469713 0.827 0.160 19 19417997 intron variant A/G snv 0.44 6