Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2072668 0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs5751129 0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs6504950 0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs7726159 0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 6
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22