| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs750496798 | 1.000 | 0.120 | 4 | 1002383 | missense variant | C/T | snv | 8.3E-06 | 1 | ||
| rs121965024 | 1.000 | 0.120 | 4 | 1002392 | missense variant | A/C | snv | 4.3E-06 | 1 | ||
| rs762903007 | 0.882 | 0.120 | 4 | 1002435 | missense variant | A/G | snv | 1.8E-05 | 7.0E-06 | 2 | |
| rs754949360 | 0.925 | 0.120 | 4 | 1002444 | missense variant | G/A | snv | 3.3E-05 | 7.0E-06 | 1 | |
| rs1553917309 | 1.000 | 0.120 | 4 | 1002450 | missense variant | C/G | snv | 1 | |||
| rs794727896 | 1.000 | 0.120 | 4 | 1002459 | missense variant | C/A;G;T | snv | 6.5E-06 | 1 | ||
| rs375628794 | 1.000 | 0.080 | 13 | 100257643 | missense variant | T/A;C | snv | 1 | |||
| rs121964995 | 1.000 | 0.080 | 9 | 100264835 | missense variant | T/C | snv | 1 | |||
| rs1555370868 | 1.000 | 14 | 100276601 | missense variant | A/C | snv | 1 | ||||
| rs931627770 | 0.925 | 0.120 | 4 | 1002811 | missense variant | C/A;T | snv | 2 | |||
| rs773205136 | 1.000 | 0.080 | 2 | 100294302 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs121964958 | 1.000 | 0.080 | 13 | 100301512 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs794727087 | 1.000 | 0.080 | 13 | 100301530 | missense variant | G/T | snv | 1 | |||
| rs1301904623 | 1.000 | 0.080 | 13 | 100301590 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs1443858896 | 1.000 | 0.080 | 13 | 100302982 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs121965027 | 0.882 | 0.120 | 4 | 1003102 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
| rs121965026 | 0.925 | 0.120 | 4 | 1003108 | missense variant | G/A;C | snv | 1 | |||
| rs772416503 | 0.882 | 0.120 | 4 | 1003120 | missense variant | C/G;T | snv | 1.4E-05 | 1 | ||
| rs121965021 | 0.807 | 0.320 | 4 | 1003418 | missense variant | C/G;T | snv | 5.6E-05 | 2 | ||
| rs764507146 | 1.000 | 0.120 | 3 | 10034797 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs200041907 | 1.000 | 16 | 100394 | missense variant | C/T | snv | 9.0E-05 | 2.6E-04 | 1 | ||
| rs121918339 | 1.000 | 0.120 | 12 | 100396373 | missense variant | C/T | snv | 1 | |||
| rs201989363 | 1.000 | 0.200 | X | 100406898 | missense variant | G/A;C;T | snv | 4.4E-05 | 1 | ||
| rs796052819 | 1.000 | 0.200 | X | 100406916 | missense variant | G/C | snv | 1 | |||
| rs267606933 | 1.000 | 0.200 | X | 100406927 | missense variant | G/A;C | snv | 1 |