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
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
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
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1333047 0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs1537378 0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs7859727 1.000 0.080 9 22102166 intron variant C/T snv 0.57 3