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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306