Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057516319 1.000 0.120 11 6615449 stop gained G/T snv 1
rs1057516366 1.000 0.120 11 6617052 frameshift variant -/A delins 1
rs1057516511 1.000 0.120 11 6614687 splice acceptor variant C/T snv 7.0E-06 1
rs1057516579 1.000 0.120 11 6614576 frameshift variant -/G delins 1
rs1057516667 1.000 0.120 11 6617777 splice acceptor variant C/G;T snv 1
rs1057517313 1.000 0.120 11 6616728 frameshift variant G/- delins 1
rs119455953 1.000 0.120 11 6616057 missense variant A/G snv 7.0E-06 1
rs119455958 1.000 0.120 11 6616690 missense variant T/C snv 4.0E-06 1
rs1218678626 1.000 0.120 11 6617037 missense variant A/G snv 4.0E-06 1
rs121908195 1.000 0.120 11 6618776 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs121908196 1.000 0.120 11 6616687 missense variant A/T snv 1
rs121908197 1.000 0.120 11 6616363 missense variant C/T snv 7.6E-05 8.4E-05 1
rs121908198 1.000 0.120 11 6615554 missense variant A/T snv 1
rs121908201 1.000 0.120 11 6615235 missense variant G/T snv 1
rs121908203 1.000 0.120 11 6615179 missense variant C/T snv 4.0E-06 1.4E-05 1
rs121908204 1.000 0.120 11 6617626 missense variant C/A;T snv 1.2E-05 1
rs121908205 1.000 0.120 11 6617057 missense variant G/A snv 1
rs121908206 1.000 0.120 11 6616333 missense variant T/G snv 1
rs121908207 1.000 0.120 11 6616718 missense variant C/T snv 1
rs121908208 1.000 0.120 11 6614973 missense variant C/G snv 1
rs121908210 1.000 0.120 11 6614608 missense variant G/A snv 1
rs1407106889 1.000 0.120 11 6615203 frameshift variant GT/- delins 1
rs1424116749 1.000 0.120 11 6616076 splice acceptor variant T/A;C snv 1
rs1554901463 1.000 0.120 11 6614617 frameshift variant GACCAGAGCAG/- delins 1
rs1554901576 1.000 0.120 11 6615228 frameshift variant GA/- delins 1