Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 6
rs6475606 0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 5
rs944797 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs523096 0.827 0.080 9 22019130 intron variant A/G snv 0.30 5
rs7049105 0.807 0.120 9 22028802 intron variant A/G snv 0.58 5
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 5
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 4
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 4
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs1333046 0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs10965219 0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs10120688 0.807 0.080 9 22056500 intron variant G/A snv 0.50 4
rs10811650 0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs1537375 0.882 0.120 9 22116072 intron variant T/C;G snv 4
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 4
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 4
rs10757272 0.851 0.160 9 22088261 intron variant C/T snv 0.41 3