Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs2516509 0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs479536 0.882 0.200 6 32225901 upstream gene variant G/A snv 5.0E-02 3
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13