Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9