Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs10408163 19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs1358980 6 43796814 intergenic variant C/T snv 0.40 6
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 5
rs1936807 6 127127104 intron variant C/G snv 0.55 4
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 4
rs718314 0.882 0.120 12 26300350 intron variant A/G snv 0.27 4
rs4738141 8 71557507 intron variant A/G snv 0.41 3