Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5