| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
| rs2236225 | 0.614 | 0.640 | 14 | 64442127 | missense variant | G/A | snv | 0.44 | 0.38 | 52 | |
| rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 17 | |
| rs2231137 | 0.752 | 0.400 | 4 | 88139962 | missense variant | C/T | snv | 0.11 | 7.4E-02 | 13 | |
| rs2230774 | 0.807 | 0.240 | 2 | 11218994 | missense variant | G/C;T | snv | 0.49 | 12 | ||
| rs193922680 | 0.790 | 0.080 | 15 | 34793398 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 9 | |
| rs6489957 | 0.925 | 0.120 | 12 | 114355808 | synonymous variant | G/A | snv | 4.4E-03 | 1.7E-02 | 4 | |
| rs1406275331 | 1.000 | 0.080 | 8 | 11708394 | missense variant | C/G;T | snv | 2 | |||
| rs397517251 | 10 | 90916262 | missense variant | G/A | snv | 5.9E-04 | 1.5E-04 | 1 | |||
| rs1037630475 | 5 | 123090099 | missense variant | C/T | snv | 1.4E-05 | 4.2E-05 | 1 | |||
| rs11041321 | 11 | 7332638 | intron variant | C/T | snv | 1.0E-01 | 1 |