Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
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
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32