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 34
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6