Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
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
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs2292239 0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs5030737 0.752 0.360 10 52771482 missense variant G/A snv 5.6E-02 5.0E-02 11
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs11171739 0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 10
rs280519 0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs1800451 0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9
rs10758593 0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs10814916 0.851 0.200 9 4293150 intron variant A/C snv 0.57 7
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs2492358 0.851 0.160 9 34737831 intron variant C/T snv 0.78 5
rs3129843 0.827 0.160 6 32427949 intergenic variant A/G snv 6.3E-02 5
rs6738825 0.851 0.200 2 198032171 intron variant A/G snv 0.49 5
rs7572733 0.925 0.120 2 198065082 intron variant C/T snv 0.43 4