Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34