Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306