Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs1412834 0.790 0.080 9 22110132 intron variant T/C snv 0.64 9
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs634537 0.851 0.080 9 22032153 intron variant T/G snv 0.28 4
rs10738607 0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 3
rs2157719 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs944801 0.882 0.120 9 22051671 intron variant G/A;C snv 3
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 3
rs10757272 0.851 0.160 9 22088261 intron variant C/T snv 0.41 2
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs1333037 0.925 0.040 9 22040766 intron variant C/T snv 0.71 2
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 2
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 2
rs2891168 0.851 0.160 9 22098620 intron variant A/G snv 0.40 2
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 2
rs7859727 1.000 0.080 9 22102166 intron variant C/T snv 0.57 2
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 2
rs10733376 1.000 0.080 9 22114470 intron variant G/C snv 0.64 1
rs10757269 1.000 0.040 9 22072265 intron variant A/C;G snv 1
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 1