Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16