Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397515947 | 1.000 | 0.040 | 11 | 47339376 | frameshift variant | G/- | delins | 2 | |||
rs199476320 | 0.925 | 0.040 | 15 | 63064121 | missense variant | C/G;T | snv | 3 | |||
rs727502886 | 0.925 | 0.040 | 1 | 236719007 | missense variant | G/A | snv | 3 | |||
rs104893823 | 0.882 | 0.040 | 3 | 52451285 | missense variant | C/T | snv | 5 | |||
rs121917776 | 0.882 | 0.040 | 10 | 74112086 | missense variant | C/T | snv | 9.9E-05 | 7.0E-06 | 5 | |
rs199476314 | 0.882 | 0.040 | 15 | 63060930 | missense variant | T/G | snv | 4 | |||
rs727503204 | 0.882 | 0.080 | 11 | 47343020 | splice donor variant | C/G;T | snv | 5 | |||
rs758264780 | 0.882 | 0.040 | 15 | 63044029 | frameshift variant | G/- | delins | 4 | |||
rs104894501 | 0.851 | 0.040 | 15 | 63044030 | stop gained | G/A;C;T | snv | 4.0E-06 | 5 | ||
rs121913627 | 0.851 | 0.080 | 14 | 23427657 | missense variant | C/A;G;T | snv | 4.0E-06 | 8 | ||
rs121913630 | 0.851 | 0.080 | 14 | 23425814 | missense variant | G/A;C | snv | 1.2E-05 | 7 | ||
rs199476301 | 0.851 | 0.040 | 15 | 63042874 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
rs606231324 | 0.851 | 0.080 | 14 | 23428505 | missense variant | C/G;T | snv | 5 | |||
rs61444459 | 0.851 | 0.160 | 1 | 156137667 | missense variant | G/A;C | snv | 5 | |||
rs150821281 | 0.827 | 0.080 | 12 | 32878461 | missense variant | G/A | snv | 2.3E-03 | 2.5E-03 | 7 | |
rs45586240 | 0.827 | 0.080 | 1 | 201361989 | missense variant | G/A;T | snv | 4.0E-06 | 7 | ||
rs74315379 | 0.827 | 0.080 | 1 | 201364336 | missense variant | G/A;T | snv | 1.2E-04 | 6 | ||
rs111033560 | 0.807 | 0.040 | 6 | 118559037 | stop gained | T/G | snv | 1.6E-05 | 9 | ||
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 |