Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs7607980 1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs10245353 7 25818994 intergenic variant C/A snv 0.16 4