Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
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
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15