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
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
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
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
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
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21