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
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
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
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
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
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs2157719 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
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
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
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
rs4841132 8 9326086 non coding transcript exon variant A/G snv 0.89 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
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11