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 60
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1412834 0.790 0.080 9 22110132 intron variant T/C snv 0.64 11
rs1333047 0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs10120688 0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs10811656 0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs523096 0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs7049105 0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs10757272 0.851 0.160 9 22088261 intron variant C/T snv 0.41 6