Source: UNIPROT ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 5 | |
| rs104893902 | 0.925 | 0.080 | 5 | 173232888 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
| rs104893904 | 0.807 | 0.160 | 5 | 173235023 | missense variant | C/G | snv | 1.1E-03 | 7.1E-04 | 2 | |
| rs104893905 | 0.925 | 0.080 | 5 | 173232898 | missense variant | G/A | snv | 4.4E-06 | 2 | ||
| rs201442000 | 0.925 | 0.080 | 5 | 173235019 | missense variant | T/C;G | snv | 1.3E-04; 4.1E-06 | 2 | ||
| rs104893900 | 1.000 | 5 | 173233011 | missense variant | G/A | snv | 1 | ||||
| rs104893906 | 1.000 | 5 | 173232976 | missense variant | G/A | snv | 1 | ||||
| rs1184594159 | 1.000 | 5 | 173233147 | missense variant | G/A | snv | 1 | ||||
| rs1223599871 | 1.000 | 5 | 173232708 | missense variant | G/A | snv | 4.1E-06 | 1 | |||
| rs137852683 | 0.925 | 5 | 173232648 | missense variant | T/C | snv | 1 | ||||
| rs137852686 | 0.851 | 0.080 | 5 | 173232997 | missense variant | T/C | snv | 1 | |||
| rs368366482 | 1.000 | 5 | 173232721 | missense variant | G/A;C;T | snv | 4.2E-06; 9.7E-05 | 1 | |||
| rs387906773 | 1.000 | 5 | 173235040 | missense variant | T/A | snv | 1 | ||||
| rs387906774 | 1.000 | 5 | 173233164 | missense variant | G/C;T | snv | 4.3E-06 | 1 | |||
| rs530270916 | 1.000 | 5 | 173234896 | missense variant | G/A;T | snv | 1.8E-05; 4.4E-06 | 1 | |||
| rs753937287 | 1.000 | 5 | 173234933 | missense variant | A/G | snv | 4.2E-06 | 1 | |||
| rs760528062 | 1.000 | 5 | 173232868 | missense variant | C/T | snv | 4.3E-06 | 1 | |||
| rs779548360 | 1.000 | 5 | 173234951 | missense variant | A/C;G | snv | 4.2E-06 | 1 |