Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554108431
DSP
0.882 0.120 6 7581189 stop gained C/T snv 4
rs397516943
DSP
0.882 0.120 6 7559281 stop gained C/G;T snv 8.0E-06 4
rs587782927
DSP
0.882 0.080 6 7574084 splice region variant AG/- delins 4
rs1553265736 0.925 0.040 1 156136080 missense variant G/C snv 4
rs267607581 0.925 0.080 1 156137651 splice region variant C/G snv 4
rs28933091 0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs58596362 0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 4
rs60682848 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 4
rs397516089 0.827 0.080 14 23429807 missense variant C/G;T snv 4
rs397516165 0.925 0.080 14 23424118 missense variant C/G;T snv 4
rs143139258 0.882 0.080 12 110913097 missense variant T/G snv 2.0E-04 2.9E-04 4
rs1554093433 0.925 0.080 5 173232833 stop gained G/T snv 4
rs1114167453 1.000 19 45385569 stop gained G/C snv 4
rs267607004 0.925 0.040 10 110812304 missense variant G/A snv 1.4E-05 4
rs397516471 0.882 0.080 1 201363348 missense variant C/T snv 4
rs45578238 0.882 0.080 1 201361971 inframe deletion CTT/- delins 4
rs727503512 0.851 0.080 1 201363349 missense variant G/A;C;T snv 4.0E-06 4
rs74315380 0.851 0.080 1 201364366 missense variant G/A;C snv 4
rs199476317 0.827 0.080 15 63062263 missense variant G/A snv 4
rs397516373 0.925 0.080 15 63059663 missense variant G/A snv 4
rs1553707780 0.925 0.040 2 178616928 frameshift variant T/- del 4
rs72648250 0.882 0.160 2 178548460 stop gained G/A;T snv 4.0E-06; 8.1E-06 4
rs727503607 0.882 0.160 2 178605642 stop gained C/A snv 4
rs397517735 0.925 0.160 2 178559309 splice donor variant A/T snv 4.4E-06 4.9E-05 4
rs72646846 0.925 0.160 2 178589849 stop gained G/A snv 7.6E-05 6.3E-05 4