Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs1569686 0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs2072668 0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14
rs5751129 0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11