Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs1042779 0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 3
rs10950398 1.000 0.040 7 12225245 intron variant G/A snv 0.52 2
rs2019065 1.000 0.040 3 52775509 upstream gene variant T/C snv 0.43 2
rs2286798 1.000 0.040 3 52787161 intron variant A/C snv 0.38 0.37 2