Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19