| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800549 | 0.925 | 0.040 | 1 | 94030497 | missense variant | G/A | snv | 4.6E-03 | 1.6E-03 | 1 | |
| rs886044720 | 0.925 | 0.080 | 1 | 94112973 | missense variant | A/C | snv | 1 | |||
| rs61750654 | 0.925 | 0.120 | 1 | 94000870 | stop gained | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs1801466 | 1.000 | 1 | 94010911 | missense variant | T/A | snv | 4.3E-02 | 4.1E-02 | 3 | ||
| rs3112831 | 1.000 | 0.080 | 1 | 94078678 | missense variant | T/C;G | snv | 0.26 | 0.26 | 2 | |
| rs752160946 | 1.000 | 0.040 | 1 | 94010868 | missense variant | C/G;T | snv | 4.0E-06; 2.8E-05 | 1 | ||
| rs1800555 | 1.000 | 0.040 | 1 | 93998061 | missense variant | C/T | snv | 1.1E-02 | 1.0E-02 | 1 | |
| rs756840095 | 1.000 | 1 | 94042797 | missense variant | G/A | snv | 2.4E-05 | 6.3E-05 | 1 | ||
| rs121909205 | 1.000 | 1 | 94120994 | missense variant | G/A;T | snv | 1.6E-05; 3.6E-05 | 1 | |||
| rs760549861 | 1.000 | 1 | 94014685 | missense variant | G/A | snv | 7.6E-05 | 7.0E-06 | 1 | ||
| rs139250920 | 1.000 | 0.080 | 1 | 94055212 | missense variant | G/A | snv | 1.7E-04 | 2.8E-04 | 1 | |
| rs61753029 | 1.000 | 1 | 94014590 | missense variant | T/C | snv | 3.2E-05 | 1 | |||
| rs781716640 | 1.000 | 1 | 94080709 | missense variant | G/A | snv | 2.0E-05 | 1.4E-05 | 1 |