Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25