Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17