Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
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
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
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
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
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
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
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29