Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614