Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
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
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs2069718 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs3824662 0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs4581 0.851 0.160 17 66214639 missense variant C/A;G snv 0.38; 4.0E-06; 4.0E-06 0.36 5
rs1051169 0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5