Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 13
rs398124146 0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs121908390 0.807 0.200 16 50796443 stop gained C/G;T snv 4.0E-06 8
rs1057519961 0.851 0.240 2 197402759 missense variant C/T snv 4
rs775623976 0.851 0.240 2 197402760 missense variant G/A;C snv 4.0E-06 4
rs587778223 0.925 0.120 16 50784435 missense variant G/A snv 3.2E-05 2.1E-05 2
rs1555913337 1.000 0.040 X 40054273 frameshift variant TAGAAGTCCCAAGTGC/- del 1