Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 24 | ||
rs1218912272 | 0.925 | 0.160 | 1 | 152314342 | stop gained | T/A | snv | 4.0E-06 | 8 | ||
rs558269137 | 0.851 | 0.160 | 1 | 152312601 | frameshift variant | ACTG/- | delins | 1.3E-02 | 8 | ||
rs372754256 | 1.000 | 1 | 152307855 | stop gained | G/C | snv | 4.7E-04 | 9.8E-05 | 3 | ||
rs121909626 | 0.882 | 0.120 | 1 | 152307225 | stop gained | G/C;T | snv | 2.0E-05 | 2 | ||
rs200519781 | 1.000 | 0.080 | 1 | 152311565 | frameshift variant | T/- | del | 2.9E-04 | 2 | ||
rs138726443 | 0.790 | 0.200 | 1 | 152307547 | stop gained | G/A;C;T | snv | 2.8E-03; 4.0E-06; 1.6E-05 | 2 | ||
rs1214424848 | 0.925 | 0.120 | 1 | 152314399 | stop gained | C/A;T | snv | 8.0E-06 | 2 | ||
rs1060499587 | 1.000 | 0.080 | 1 | 152313983 | frameshift variant | TCCTG/- | delins | 1 | |||
rs115746363 | 0.882 | 0.120 | 1 | 152312410 | stop gained | G/A;C | snv | 6.0E-04 | 1 | ||
rs535289422 | 1.000 | 0.080 | 1 | 152307697 | stop gained | G/A;C | snv | 1.6E-05; 4.0E-06 | 1 | ||
rs149484917 | 0.882 | 0.120 | 1 | 152304939 | stop gained | G/C;T | snv | 4.7E-04; 4.0E-06 | 1 | ||
rs761212672 | 0.882 | 0.120 | 1 | 152304999 | stop gained | G/T | snv | 3.2E-05 | 1 | ||
rs754812742 | 1.000 | 0.080 | 1 | 152310981 | stop gained | G/A;T | snv | 2.4E-05; 1.2E-04 | 1 | ||
rs797045090 | 1.000 | 0.080 | 1 | 152312743 | stop gained | G/A | snv | 1 | |||
rs150597413 | 0.827 | 0.160 | 1 | 152305146 | stop gained | G/A;C;T | snv | 3.6E-05; 4.0E-06; 1.5E-03 | 1 | ||
rs114733570 | 1.000 | 0.080 | 1 | 152315363 | stop gained | C/A | snv | 1.2E-04 | 2.0E-04 | 1 | |
rs141784184 | 1.000 | 0.080 | 1 | 152309169 | stop gained | G/A;T | snv | 8.0E-06; 1.6E-03 | 1 | ||
rs747301529 | 1.000 | 0.120 | 1 | 152309716 | stop gained | C/A | snv | 4.0E-06 | 1 |