Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1129844 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59