Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893823 0.882 0.040 3 52451285 missense variant C/T snv 1
rs104894501 0.851 0.040 15 63044030 stop gained G/A;C;T snv 4.0E-06 1
rs104894505 0.882 0.040 15 63044072 missense variant G/A snv 1
rs104894655 0.925 0.120 17 39665762 stop gained C/T snv 1.4E-05 3
rs104894942 1.000 0.120 X 154413248 missense variant C/A;T snv 1
rs1064793814 2 178559769 stop gained C/T snv 1
rs111033559 0.925 0.040 6 118558946 missense variant C/T snv 3
rs111033560 0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 7
rs1114167453 1.000 19 45385569 stop gained G/C snv 4
rs111569862 1 156137653 splice acceptor variant G/A;C snv 1
rs112188483 0.925 0.160 2 178528273 splice donor variant C/G;T snv 1.2E-05 3
rs112240298 2 178538945 splice donor variant C/G;T snv 1
rs114638163 0.827 0.240 13 23805994 stop gained C/A;T snv 4.0E-06; 1.3E-03 10
rs121912997
DSP
0.925 0.160 6 7579989 stop gained C/G;T snv 3
rs121913627 0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 3
rs121913630 0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 3
rs121913642 0.925 0.080 14 23427879 missense variant A/G snv 3
rs121913647 0.925 0.160 14 23417173 missense variant C/A;G;T snv 1.6E-05 3
rs137853197 0.925 0.040 1 77942756 missense variant A/G snv 7.2E-05 1.0E-04 3
rs137854618 0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 5
rs140614802 0.851 0.040 14 104741231 missense variant G/A snv 3.4E-05 2.8E-05 10
rs140743001 1.000 0.040 2 178630250 stop gained G/A snv 8.1E-06 1.4E-05 2
rs1408345511 2 178740175 frameshift variant G/- delins 4.0E-06 1
rs143139258 0.882 0.080 12 110913097 missense variant T/G snv 2.0E-04 2.9E-04 4
rs145734640 0.925 0.080 14 23415096 missense variant G/A;C;T snv 1.6E-05; 1.6E-05; 4.0E-06 1