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
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
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
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
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
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
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