Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs12720270 0.851 0.240 19 10365084 intron variant G/A snv 0.21 0.16 4
rs280500 0.882 0.200 19 10379726 5 prime UTR variant A/G snv 0.20 3
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
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
rs929763 0.925 0.160 5 170783993 intron variant A/T snv 0.72 2
rs3805455 0.925 0.160 5 170813490 3 prime UTR variant T/C snv 0.50 2
rs10489265 0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
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
rs2243188 0.851 0.200 1 206841127 intron variant A/C;T snv 0.69 4
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1051169 0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5