Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs20417 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 57 | |||
| rs5275 | 0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv | 55 | |||
| rs689466 | 0.637 | 0.640 | 1 | 186681619 | upstream gene variant | T/C | snv | 0.17 | 33 | ||
| rs5277 | 0.790 | 0.160 | 1 | 186679065 | synonymous variant | C/G;T | snv | 0.12; 8.0E-06 | 9 | ||
| rs748500299 | 0.790 | 0.200 | 1 | 186675960 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 8 | ||
| rs5273 | 0.827 | 0.080 | 1 | 186674636 | missense variant | A/C;G | snv | 4.0E-06; 7.6E-03 | 1.4E-02 | 6 | |
| rs4648298 | 0.882 | 0.120 | 1 | 186672550 | 3 prime UTR variant | T/C | snv | 1.7E-02 | 3 | ||
| rs13306035 | 1.000 | 0.080 | 1 | 186672715 | 3 prime UTR variant | A/G | snv | 1 | |||
| rs377655174 | 1.000 | 0.080 | 1 | 186678374 | missense variant | G/A | snv | 8.1E-06 | 1 | ||
| rs5276 | 1.000 | 0.080 | 1 | 186673855 | 3 prime UTR variant | C/T | snv | 4.6E-02 | 1 | ||
| rs20426 | 1.000 | 0.080 | 1 | 186680288 | start lost | C/T | snv | 1 |