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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs1042173 0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs165774 0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27 11
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 6