Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs72915971 1.000 0.080 11 57158067 intergenic variant C/G snv 2.4E-02 2