Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs17145750 0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs1051921 0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs3823418 0.925 0.120 6 31133165 intron variant G/A snv 0.23 6
rs17145738 0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5