Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs6475606 0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs944797 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 4
rs1333046 0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs10738609 1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 3