Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs759834538 0.925 0.120 9 136517294 missense variant C/A snv 1.7E-05 3
rs587781386 0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3
rs764562217 0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs752626029 0.925 0.120 2 25239208 missense variant G/A;C;T snv 4.0E-06; 1.2E-05; 4.0E-06 2
rs572432356 0.925 0.120 5 75596681 missense variant A/C snv 2
rs35631544 0.925 0.120 16 24191130 missense variant C/A;G snv 6.3E-04 1.0E-03 2
rs1157200929 0.925 0.120 19 22180315 stop gained T/A snv 2
rs72963007 1.000 0.120 4 105243566 splice region variant G/A snv 3.2E-03 1.0E-02 1