| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 42 | |||
| rs1553920379 | 0.776 | 0.160 | 4 | 101032294 | frameshift variant | -/AGTA | delins | 27 | |||
| rs6259 | 0.658 | 0.400 | 17 | 7633209 | missense variant | G/A | snv | 8.9E-02 | 8.1E-02 | 27 | |
| rs1208636573 | 0.807 | 0.120 | 1 | 155612098 | stop gained | C/G;T | snv | 4.0E-06; 4.0E-06 | 15 | ||
| rs622288 | 0.807 | 0.120 | 1 | 155612848 | missense variant | C/T | snv | 3.6E-05 | 4.2E-05 | 15 | |
| rs2710102 | 0.790 | 0.120 | 7 | 147877298 | intron variant | A/G;T | snv | 12 | |||
| rs63749855 | 0.790 | 0.200 | 17 | 46014271 | missense variant | T/G | snv | 8 | |||
| rs7794745 | 0.851 | 0.040 | 7 | 146792514 | intron variant | A/T | snv | 0.49 | 6 | ||
| rs9901675 | 17 | 7581494 | missense variant | G/A | snv | 5.4E-02 | 5.5E-02 | 5 | |||
| rs762046989 | 0.851 | 0.200 | 17 | 45971867 | missense variant | C/G | snv | 8.0E-06 | 5 | ||
| rs63749891 | 0.851 | 0.080 | 14 | 73198094 | missense variant | G/C;T | snv | 5 | |||
| rs533813519 | 0.851 | 0.120 | 1 | 226888097 | missense variant | C/A | snv | 1.9E-04 | 4.2E-05 | 5 | |
| rs1569540688 | 0.925 | 0.240 | X | 153725586 | missense variant | T/C | snv | 4 | |||
| rs2230365 | 0.925 | 0.160 | 6 | 31557671 | synonymous variant | C/T | snv | 0.16 | 0.13 | 4 | |
| rs533667466 | 0.925 | 0.080 | 21 | 25911912 | missense variant | T/C | snv | 3 | |||
| rs63750072 | 1.000 | 0.080 | 17 | 45983493 | missense variant | A/G | snv | 4.0E-02 | 3.8E-02 | 3 | |
| rs63749961 | 0.925 | 0.080 | 14 | 73192772 | missense variant | T/G | snv | 3 | |||
| rs142690225 | 0.925 | 0.080 | 1 | 226894111 | missense variant | G/A | snv | 1.1E-04 | 1.1E-04 | 3 | |
| rs1287723181 | 1.000 | 0.080 | 21 | 25954680 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs202218688 | 1.000 | 0.080 | 21 | 26000131 | missense variant | C/A;T | snv | 4.0E-06; 5.6E-05 | 2 | ||
| rs200754713 | 1 | 226888954 | missense variant | A/G | snv | 4.0E-06; 4.0E-06 | 2 | ||||
| rs3734354 | 1.000 | 0.080 | 6 | 100420903 | missense variant | G/A;T | snv | 1.6E-04; 0.18 | 2 | ||
| rs1470272477 | 1.000 | 0.080 | 12 | 64495561 | missense variant | G/C | snv | 2 | |||
| rs2239707 | 6 | 31557542 | intron variant | C/A;G;T | snv | 1 | |||||
| rs144169475 | 4 | 47905303 | missense variant | A/T | snv | 7.1E-03 | 3.4E-03 | 1 |