Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs4988235 0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
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
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249