Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs10761731 10 63267850 intron variant A/T snv 0.38 6
rs2375980 9 2692622 intergenic variant C/G snv 0.51 3
rs113600793 17 47384095 intron variant C/A;T snv 3
rs2393967 10 63373396 intron variant A/C snv 0.23 3
rs4349809 6 43957093 intergenic variant T/A;G snv 2
rs145593549 6 44160144 intron variant A/T snv 6.8E-03 2
rs2893923 10 63501424 intron variant C/T snv 0.27 2
rs12199215 6 44059177 non coding transcript exon variant C/T snv 0.25 2
rs72831623 17 47644927 intron variant G/A;C snv 4.0E-02 2
rs192137842 9 107505575 regulatory region variant G/A snv 1.3E-03 1