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
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs10968576 0.882 0.120 9 28414341 intron variant A/G snv 0.26 10