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
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
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
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
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
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
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28