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 24
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs4823006 22 29055683 3 prime UTR variant A/G snv 0.41 5
rs166840 17 19896385 downstream gene variant G/A snv 0.36 2
rs2300481 2 66555335 intron variant C/T snv 0.36 2