Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1060503526 | 0.925 | 0.120 | 4 | 88038380 | stop gained | C/T | snv | 1.2E-05 | 2 | ||
rs11122577 | 1.000 | 0.120 | 1 | 230711810 | intron variant | C/A | snv | 0.19 | 2 | ||
rs1131692280 | 0.925 | 0.120 | 4 | 88043458 | splice donor variant | G/A | snv | 8.0E-06 | 1.4E-05 | 3 | |
rs1187336837 | 1.000 | 0.120 | 4 | 88007931 | frameshift variant | C/-;CC | delins | 1 | |||
rs121918040 | 0.925 | 0.120 | 4 | 88065479 | stop gained | C/T | snv | 7.0E-06 | 2 | ||
rs121918043 | 0.925 | 0.120 | 4 | 88046854 | missense variant | A/T | snv | 2 | |||
rs1222213359 | 0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv | 62 | |||
rs1232369409 | 1.000 | 0.120 | 4 | 88008244 | frameshift variant | G/- | delins | 7.0E-06 | 1 | ||
rs1249050389 | 0.925 | 0.240 | 9 | 95485696 | stop gained | G/C | snv | 2 | |||
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs1302726543 | 0.925 | 0.120 | 4 | 88019499 | stop gained | C/T | snv | 7.0E-06 | 2 | ||
rs1391596181 | 1.000 | 0.120 | 4 | 88046647 | stop gained | T/A;C | snv | 4.0E-06 | 1 | ||
rs1392093609 | 1.000 | 0.120 | 4 | 88007759 | missense variant | C/T | snv | 1 | |||
rs1464816 | 1.000 | 0.120 | 1 | 204159726 | intron variant | T/C;G | snv | 2 | |||
rs1487813753 | 1.000 | 0.120 | 10 | 100293336 | missense variant | T/C;G | snv | 8.0E-06 | 1 | ||
rs1553925453 | 0.925 | 0.120 | 4 | 88038371 | missense variant | C/T | snv | 2 | |||
rs1553926509 | 1.000 | 0.120 | 4 | 88052018 | frameshift variant | TA/- | delins | 1 | |||
rs1553926905 | 1.000 | 0.120 | 4 | 88056143 | stop gained | C/T | snv | 1 | |||
rs1553927080 | 1.000 | 0.120 | 4 | 88058104 | splice donor variant | G/A | snv | 1 | |||
rs1555452849 | 1.000 | 0.120 | 16 | 2106172 | frameshift variant | G/- | delins | 1 | |||
rs1560592253 | 1.000 | 0.120 | 4 | 88008174 | frameshift variant | G/- | delins | 1 | |||
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
rs4362 | 0.807 | 0.240 | 17 | 63496400 | missense variant | T/C;G | snv | 0.52; 1.2E-05 | 0.51 | 9 | |
rs4762 | 0.637 | 0.440 | 1 | 230710231 | missense variant | G/A | snv | 0.12 | 0.11 | 35 |