Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs6330 0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs137852642 0.827 0.200 19 15192242 missense variant G/A;T snv 4.5E-06; 4.5E-06 9