Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 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
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
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
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26