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
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
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
rs1051169 0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5
rs2243188 0.851 0.200 1 206841127 intron variant A/C;T snv 0.69 4
rs741761 0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs3181032 0.925 0.160 12 68162395 intron variant A/C snv 5.3E-02 2
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs12720270 0.851 0.240 19 10365084 intron variant G/A snv 0.21 0.16 4
rs28362930 0.925 0.160 15 74408859 downstream gene variant G/A snv 0.16 3
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs280500 0.882 0.200 19 10379726 5 prime UTR variant A/G snv 0.20 3
rs10489265 0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16