Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1060499548 | 0.724 | 0.440 | 9 | 130872961 | missense variant | G/A | snv | 27 | |||
rs1060505041 | 0.716 | 0.400 | 19 | 13136099 | missense variant | C/A;T | snv | 34 | |||
rs1064795104 | 0.790 | 0.440 | 2 | 72498492 | stop gained | A/C | snv | 17 | |||
rs1064796765 | 0.763 | 0.240 | 14 | 102002950 | missense variant | G/A | snv | 19 | |||
rs1085307135 | 0.882 | 0.160 | 8 | 143818255 | missense variant | C/T | snv | 5 | |||
rs1085307138 | 0.807 | 0.160 | 8 | 143817591 | splice donor variant | C/T | snv | 9 | |||
rs1085307139 | 0.925 | 0.040 | 8 | 143817380 | frameshift variant | -/C | delins | 5 | |||
rs1131691804 | 0.807 | 0.200 | 15 | 48463123 | missense variant | G/A | snv | 6 | |||
rs1131692272 | 0.851 | 0.240 | 2 | 100006808 | missense variant | C/T | snv | 8 | |||
rs113993993 | 0.851 | 0.040 | 7 | 66994210 | splice donor variant | A/C;G | snv | 4.0E-06; 3.9E-03 | 9 | ||
rs114925667 | 0.672 | 0.520 | 3 | 132675903 | missense variant | G/A;T | snv | 1.9E-03; 4.1E-06 | 62 | ||
rs1158061584 | 13 | 32443086 | frameshift variant | T/-;TT | delins | 1 | |||||
rs119103263 | 0.827 | 0.240 | 1 | 11992659 | missense variant | C/T | snv | 17 | |||
rs119473033 | 0.827 | 0.320 | 2 | 216478216 | stop gained | G/T | snv | 8.0E-05 | 1.3E-04 | 11 | |
rs120074160 | 0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 | 6 | ||
rs121434616 | 0.925 | 0.080 | X | 120544179 | stop gained | G/A | snv | 6 | |||
rs121908216 | 0.882 | 0.200 | 19 | 13235702 | missense variant | C/T | snv | 7 | |||
rs121912651 | 0.605 | 0.680 | 17 | 7674221 | missense variant | G/A;C | snv | 4.0E-06 | 37 | ||
rs121912854 | 0.851 | 0.200 | 3 | 48592915 | stop gained | G/A | snv | 1.2E-05 | 7.0E-06 | 16 | |
rs121912855 | 0.851 | 0.200 | 3 | 48575218 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 15 | |
rs121913115 | 1.000 | 0.120 | 4 | 1801928 | missense variant | A/G | snv | 2 | |||
rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 35 | |||
rs121913528 | 0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv | 11 | |||
rs121918454 | 0.742 | 0.280 | 12 | 112450395 | missense variant | C/A;G;T | snv | 16 | |||
rs121918457 | 0.701 | 0.280 | 12 | 112488466 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 18 |