Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3218716 | 0.716 | 0.280 | 14 | 23425316 | missense variant | C/A;G;T | snv | 4.0E-06; 2.4E-05 | 17 | ||
rs121913628 | 0.763 | 0.160 | 14 | 23424059 | missense variant | C/G;T | snv | 10 | |||
rs3218713 | 0.763 | 0.160 | 14 | 23431468 | missense variant | C/A;T | snv | 10 | |||
rs587782958 | 0.790 | 0.120 | 11 | 47333552 | splice region variant | C/T | snv | 1.7E-05 | 10 | ||
rs3218714 | 0.763 | 0.160 | 14 | 23429279 | missense variant | G/A;C | snv | 9 | |||
rs397516127 | 0.763 | 0.160 | 14 | 23426834 | missense variant | G/A;C | snv | 9 | |||
rs397516171 | 0.763 | 0.160 | 14 | 23424041 | missense variant | C/G;T | snv | 9 | |||
rs397516264 | 0.763 | 0.160 | 14 | 23431602 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs397516354 | 0.790 | 0.120 | 19 | 55154094 | missense variant | C/A;G;T | snv | 4.0E-05 | 7 | ||
rs121908987 | 0.742 | 0.200 | 7 | 151576412 | missense variant | C/A;G;T | snv | 4.0E-06 | 6 | ||
rs121909374 | 0.790 | 0.120 | 11 | 47342578 | stop gained | C/A;G | snv | 1.3E-05 | 6 | ||
rs397516349 | 0.807 | 0.080 | 19 | 55154145 | missense variant | C/T | snv | 1.6E-05 | 6 | ||
rs727503504 | 0.807 | 0.080 | 19 | 55154071 | missense variant | G/A;C | snv | 6 | |||
rs121434594 | 0.827 | 0.160 | 3 | 12604189 | missense variant | G/A;C;T | snv | 5 | |||
rs267606910 | 0.807 | 0.080 | 14 | 23431589 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
rs36211723 | 0.851 | 0.080 | 11 | 47338520 | missense variant | C/G;T | snv | 1.6E-05 | 5 | ||
rs397516059 | 0.851 | 0.080 | 11 | 47349876 | frameshift variant | -/A | delins | 8.2E-06 | 5 | ||
rs397516248 | 0.851 | 0.200 | 14 | 23415153 | missense variant | C/T | snv | 5 | |||
rs727503166 | 0.851 | 0.080 | 11 | 47332110 | frameshift variant | T/- | del | 5 | |||
rs727503204 | 0.882 | 0.080 | 11 | 47343020 | splice donor variant | C/G;T | snv | 5 | |||
rs104894724 | 0.790 | 0.120 | 19 | 55154146 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
rs104894727 | 0.882 | 0.080 | 19 | 55151881 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs104894729 | 0.827 | 0.080 | 19 | 55151892 | missense variant | C/A;G;T | snv | 4 | |||
rs1060499604 | 0.851 | 0.080 | 11 | 47339323 | splice donor variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs199474703 | 0.851 | 0.120 | 3 | 46860702 | missense variant | C/T | snv | 8.0E-06 | 4 |