Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38