Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs1805054 0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs76980269 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10