Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs80357138 0.763 0.200 17 43094776 missense variant C/T snv 8.0E-06 9
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51