Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10