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 80
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 79
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
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
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 47
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 29
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 28
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 27
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 23
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22