Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10203174 1.000 0.080 2 43462891 intron variant C/T snv 0.17 1
rs13405158 1.000 0.080 2 43478147 intron variant T/C snv 0.17 1
rs13414381 1.000 0.080 2 43340079 intron variant T/C snv 0.18 1
rs17334919 1.000 0.080 2 43480246 intron variant C/T snv 7.0E-02 1
rs35720761 1.000 0.080 2 43292838 missense variant C/A;G;T snv 2.9E-05; 9.9E-02 1
rs6743071 1.000 0.080 2 43359148 intron variant T/C;G snv 1
rs7578597 0.807 0.240 2 43505684 missense variant T/C snv 9.9E-02 0.14 1