Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11806129 1 94016821 intron variant A/G;T snv 3
rs12087003 1 94037627 intron variant A/G snv 6.3E-02 3
rs17110922 1 94043489 intron variant A/T snv 2.5E-03 9.9E-03 2
rs1064793014 1 94007707 missense variant T/C snv 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
rs149071415 1 94047024 missense variant A/G snv 4.0E-05 8.4E-05 1
rs1553190559 1 94042790 missense variant A/T snv 1
rs1553192432 1 94060712 frameshift variant -/C delins 1
rs1557787756 1 94063158 stop gained G/A snv 1
rs61752419 1 94042786 stop gained C/T snv 1
rs776757706 1 94014688 stop gained C/T snv 4.0E-06 1
rs869312184 1 94048898 frameshift variant C/- delins 1
rs878853396 1 94062641 stop gained G/A;C snv 4.0E-06 1
rs878853397 1 94043428 frameshift variant T/- delins 1
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 10
rs61750200 0.790 0.080 1 94098928 missense variant G/A;T snv 1.1E-04; 8.0E-06 8
rs61750641 0.790 0.080 1 94005499 missense variant C/T snv 3.5E-04 4.7E-04 7
rs1800728 0.807 0.080 1 94011395 intron variant A/G snv 2.3E-04 3.0E-04 8
rs768435443 0.807 0.080 1 94055128 missense variant A/G snv 4.0E-06 8
rs61750130 0.807 0.080 1 94031110 missense variant G/A snv 2.4E-04 2.3E-04 7
rs62645944 0.807 0.080 1 94098794 splice region variant C/A snv 8.8E-05 6.3E-05 7
rs281865377 0.807 0.080 1 94029447 frameshift variant G/-;GG delins 2.1E-05 6
rs61751392 0.827 0.080 1 94063250 missense variant A/G snv 1.5E-04 1.7E-04 7