| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs119455953 | 1.000 | 0.120 | 11 | 6616057 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs119455958 | 1.000 | 0.120 | 11 | 6616690 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs1218678626 | 1.000 | 0.120 | 11 | 6617037 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs121908195 | 1.000 | 0.120 | 11 | 6618776 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs121908196 | 1.000 | 0.120 | 11 | 6616687 | missense variant | A/T | snv | 1 | |||
| rs121908197 | 1.000 | 0.120 | 11 | 6616363 | missense variant | C/T | snv | 7.6E-05 | 8.4E-05 | 1 | |
| rs121908198 | 1.000 | 0.120 | 11 | 6615554 | missense variant | A/T | snv | 1 | |||
| rs121908201 | 1.000 | 0.120 | 11 | 6615235 | missense variant | G/T | snv | 1 | |||
| rs121908203 | 1.000 | 0.120 | 11 | 6615179 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs121908204 | 1.000 | 0.120 | 11 | 6617626 | missense variant | C/A;T | snv | 1.2E-05 | 1 | ||
| rs121908205 | 1.000 | 0.120 | 11 | 6617057 | missense variant | G/A | snv | 1 | |||
| rs121908206 | 1.000 | 0.120 | 11 | 6616333 | missense variant | T/G | snv | 1 | |||
| rs121908207 | 1.000 | 0.120 | 11 | 6616718 | missense variant | C/T | snv | 1 | |||
| rs121908208 | 1.000 | 0.120 | 11 | 6614973 | missense variant | C/G | snv | 1 | |||
| rs121908210 | 1.000 | 0.120 | 11 | 6614608 | missense variant | G/A | snv | 1 | |||
| rs1424116749 | 1.000 | 0.120 | 11 | 6616076 | splice acceptor variant | T/A;C | snv | 1 | |||
| rs1554901731 | 1.000 | 0.120 | 11 | 6616075 | splice acceptor variant | C/T | snv | 1 | |||
| rs1554902028 | 1.000 | 0.120 | 11 | 6617352 | splice donor variant | A/G | snv | 1 | |||
| rs1564854729 | 1.000 | 0.120 | 11 | 6616052 | stop gained | C/T | snv | 1 | |||
| rs28940573 | 1.000 | 0.120 | 11 | 6617046 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs752164603 | 1.000 | 0.120 | 11 | 6617022 | stop gained | G/A | snv | 4.0E-06 | 1 | ||
| rs757953998 | 1.000 | 0.120 | 11 | 6616750 | missense variant | C/T | snv | 1.2E-05 | 4.2E-05 | 1 | |
| rs779615685 | 1.000 | 0.120 | 11 | 6619383 | splice donor variant | C/G;T | snv | 1 | |||
| rs786204553 | 1.000 | 0.120 | 11 | 6614865 | splice donor variant | C/A;G;T | snv | 1 | |||
| rs869025274 | 1.000 | 0.120 | 11 | 6617353 | splice donor variant | C/A;G | snv | 1 |