Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs2383205 0.925 0.080 9 22060936 intron variant A/C;G snv 3
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs6475606 0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs10738606 1.000 0.040 9 22088091 intron variant A/T snv 0.42 2
rs10757272 0.851 0.160 9 22088261 intron variant C/T snv 0.41 6
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs2891168 0.851 0.160 9 22098620 intron variant A/G snv 0.40 5
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs10738609 1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs944797 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1537376 1.000 0.040 9 22116221 intron variant T/C snv 0.49 2
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs10217586 1.000 0.040 9 22121350 intron variant A/T snv 0.52 2