Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31