Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047376 1.000 1 94041354 missense variant A/G;T snv 4.0E-06 1
rs1057518767 0.851 0.120 1 94098874 missense variant A/T snv 5
rs1057518955 1.000 0.120 1 94019602 frameshift variant -/C delins 4.1E-06 2
rs1064793013 1.000 0.080 1 94008300 splice region variant G/A;T snv 1
rs1064793014 1 94007707 missense variant T/C snv 1
rs113106943 0.925 0.040 1 94021848 missense variant C/T snv 2.4E-03 2.3E-03 2
rs11806129 1 94016821 intron variant A/G;T snv 3
rs12087003 1 94037627 intron variant A/G snv 6.3E-02 3
rs121909204 1.000 1 94043443 missense variant G/A snv 1
rs121909205 1.000 1 94120994 missense variant G/A;T snv 1.6E-05; 3.6E-05 2
rs121909206 0.925 0.080 1 94015766 missense variant G/A;T snv 4.0E-06 2
rs121909207 1.000 1 94014665 missense variant G/A;C snv 1.1E-04 1
rs1297857869 1.000 1 94011330 missense variant A/G snv 4.0E-06 1
rs1356104318 1 94098850 stop gained G/A;C snv 4.0E-06 1
rs137866734 1 94074274 intron variant C/T snv 6.8E-03 1
rs139250920 1.000 0.080 1 94055212 missense variant G/A snv 1.7E-04 2.8E-04 1
rs140482171 1.000 1 94077712 missense variant C/T snv 7.8E-04 4.1E-04 1
rs142253670 1.000 1 94008252 missense variant C/T snv 9.1E-05 7.0E-05 1
rs1435203678 1.000 1 94019690 missense variant G/A;C snv 8.0E-06 1
rs145525174 1.000 1 94063218 missense variant C/T snv 2.7E-03 2.4E-03 1
rs1457937638 1.000 1 94027444 intron variant C/A;T snv 1
rs145961131 1.000 1 94062608 stop gained G/A snv 2.0E-05 2.1E-05 1
rs148460146 1.000 1 94005469 missense variant C/T snv 3.1E-04 2.6E-04 1
rs149071415 1 94047024 missense variant A/G snv 4.0E-05 8.4E-05 1
rs150774447 1.000 1 94111579 missense variant C/A;T snv 4.0E-06; 2.4E-05 2