Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121907981 0.882 0.120 15 72345550 missense variant C/G snv 1.2E-05 7.0E-06 3
rs267606862 0.882 0.160 15 72346681 stop gained C/T snv 3
rs587779406 1.000 0.120 15 72346552 synonymous variant G/A snv 8.0E-05 1.0E-04 3
rs755973971 0.882 0.120 15 72346661 missense variant T/A;C;G snv 7.6E-05; 1.6E-05 3
rs1057519021 0.925 0.120 5 151267341 stop gained G/T snv 2
rs121907955 0.925 0.120 15 72345461 missense variant C/A;T snv 4.0E-06 2
rs121907956 0.925 0.120 15 72345476 missense variant C/T snv 5.6E-05 3.5E-05 2
rs121907958 0.925 0.120 15 72346597 missense variant C/G snv 8.0E-06 2.8E-05 2
rs121907959 0.925 0.120 15 72350574 missense variant C/A;T snv 8.0E-06 2
rs121907970 0.925 0.120 15 72350584 missense variant G/A snv 1.5E-03 1.9E-03 2
rs121907980 0.925 0.120 15 72350517 splice donor variant C/G;T snv 4.0E-06; 4.0E-06 2
rs199578185 0.925 0.120 15 72349181 missense variant T/C snv 8.0E-06 7.0E-06 2
rs28941770 0.925 0.120 15 72353105 missense variant C/A;G;T snv 4.8E-05 2
rs28941771 0.925 0.120 15 72353100 missense variant A/G snv 2
rs28942071 1.000 0.120 15 72345462 missense variant G/A snv 2.4E-05 7.0E-06 2
rs387906311 0.925 0.120 15 72351132 splice donor variant C/T snv 4.0E-06 2
rs770932296 1.000 0.120 15 72349266 splice region variant C/T snv 2.4E-05 6.3E-05 2
rs587779405 1.000 0.120 5 151266820 frameshift variant C/- del 1
rs1057516617 1.000 0.120 15 72346707 stop gained G/A;C snv 4.0E-06; 4.0E-06 1
rs1057516755 1.000 0.120 15 72348075 frameshift variant TTGA/- del 1
rs1057516850 1.000 0.120 15 72353173 frameshift variant A/- delins 1
rs1057516908 1.000 0.120 15 72349260 splice acceptor variant C/G snv 1
rs1057517174 1.000 0.120 15 72353714 frameshift variant C/- del 2.1E-05 1
rs1057519458 1.000 0.120 15 72353724 frameshift variant A/- delins 1
rs1057519459 1.000 0.120 15 72353687 splice region variant T/G snv 1