Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
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
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs121909244 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11