Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98