Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs2157719 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs10120688 0.807 0.080 9 22056500 intron variant G/A snv 0.50 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
rs2383204 0.827 0.160 9 22055049 intron variant A/G;T snv 6