Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894369 | 0.807 | 0.080 | 12 | 110914287 | missense variant | C/A;T | snv | 10 | |||
rs104894502 | 0.807 | 0.120 | 15 | 63060915 | missense variant | A/G;T | snv | 6 | |||
rs104894503 | 0.776 | 0.160 | 15 | 63060899 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 9 | |
rs104894724 | 0.790 | 0.120 | 19 | 55154146 | missense variant | G/A;C | snv | 4.0E-06 | 8 | ||
rs104894729 | 0.827 | 0.080 | 19 | 55151892 | missense variant | C/A;G;T | snv | 5 | |||
rs121913624 | 0.851 | 0.080 | 14 | 23429278 | missense variant | C/A;G;T | snv | 4 | |||
rs121913625 | 0.851 | 0.080 | 14 | 23429005 | missense variant | G/A;C;T | snv | 4 | |||
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 | ||
rs121964857 | 0.851 | 0.080 | 1 | 201359245 | missense variant | G/A | snv | 3.6E-04 | 4.3E-04 | 4 | |
rs121964858 | 0.807 | 0.120 | 1 | 201365244 | missense variant | A/C;G;T | snv | 6 | |||
rs199476321 | 0.882 | 0.080 | 15 | 63064133 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs36211715 | 0.851 | 0.080 | 14 | 23424839 | missense variant | C/A;G;T | snv | 4.0E-06 | 5 | ||
rs375882485 | 0.827 | 0.080 | 11 | 47342698 | missense variant | G/A | snv | 4.0E-05 | 9.8E-05 | 5 | |
rs397516005 | 0.827 | 0.120 | 11 | 47333566 | stop gained | G/A | snv | 8.4E-06 | 2.8E-05 | 5 | |
rs573916965 | 0.827 | 0.080 | 11 | 47346297 | stop gained | C/A;T | snv | 2.5E-04 | 5 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs775404728 | 0.851 | 0.080 | 11 | 47337535 | missense variant | G/A | snv | 4.0E-06 | 4 |