Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12363415 1.000 0.080 11 13377061 intron variant A/G snv 0.20 1
rs2073746 1.000 0.080 22 19991035 intron variant T/C snv 0.80 1
rs4901043 1.000 0.080 14 50616876 intron variant T/C snv 0.49 1
rs16980013 1.000 0.080 19 45764195 3 prime UTR variant G/T snv 0.24 1
rs754107 1.000 0.080 2 127103254 intron variant C/G snv 0.63 1
rs17512204 1.000 0.080 2 117975255 missense variant G/A snv 5.6E-02 5.3E-02 1
rs2233872 1.000 0.080 9 34691559 upstream gene variant A/G snv 0.21 1
rs11574915 1.000 0.080 9 34710087 5 prime UTR variant A/C;G snv 0.13; 4.1E-06 1
rs17237890 1.000 0.080 16 56962246 5 prime UTR variant T/C snv 1
rs1800774 1.000 0.080 16 56981633 intron variant C/A;T snv 4.0E-06; 0.32; 4.0E-06 1
rs942576 1.000 0.080 10 69903027 intron variant G/T snv 0.30 1
rs55940034 1.000 0.080 13 110390962 intron variant A/G snv 0.28 1
rs2434237 1.000 0.080 5 175797902 intron variant C/A snv 0.18 1
rs4407312 1.000 0.080 20 23826391 intron variant A/C;G;T snv 0.76; 4.1E-06; 6.6E-05 1
rs6048952 1.000 0.080 20 23626620 downstream gene variant A/G snv 0.27 1
rs1276663775 1.000 0.080 20 23879610 missense variant C/A;T snv 4.0E-06 1
rs9462875 1.000 0.080 6 43200379 intron variant A/G snv 0.24 1
rs1050998 1.000 0.080 17 4735442 missense variant A/G snv 0.46 0.41 1
rs8123 1.000 0.080 17 4733270 3 prime UTR variant T/G snv 0.22 1
rs6723449 1.000 0.080 2 218132857 intron variant T/C snv 0.62 1
rs1058932 1.000 0.080 10 95037104 3 prime UTR variant G/A snv 0.22 0.24 1
rs10889160 1.000 0.080 1 59896449 intron variant T/C snv 0.23 1
rs2271800 1.000 0.080 1 59907994 intron variant A/C;T snv 1
rs3093200 1.000 0.080 19 15878779 missense variant G/C;T snv 5.3E-02 1
rs669173 1.000 0.080 1 85433745 intron variant T/C snv 0.42 1