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
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
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
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs2227981 0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12