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
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs2112347 0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs3810291 19 47065746 3 prime UTR variant G/A snv 0.50 9
rs1516725 0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs11676272 1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 5