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
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14