Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
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
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
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
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33