Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs12446632 1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs2112347 0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs7531118 1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs2531995 1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs7141420 1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs987237 0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs17381664 1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs2030323 0.925 0.080 11 27706992 intron variant A/C snv 0.83 3
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 3