| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs199473640 | 1.000 | 0.120 | 3 | 38550338 | missense variant | G/A | snv | 4.3E-05 | 2.1E-05 | 1 | |
| rs41311117 | 0.882 | 0.120 | 3 | 38550362 | missense variant | A/C;G;T | snv | 3.6E-05; 2.0E-03; 1.0E-05 | 2 | ||
| rs199473334 | 1.000 | 0.120 | 3 | 38550443 | missense variant | A/T | snv | 1 | |||
| rs41315493 | 0.851 | 0.120 | 3 | 38550521 | missense variant | C/A;T | snv | 6.6E-03; 9.7E-05 | 3 | ||
| rs199473330 | 1.000 | 0.120 | 3 | 38550527 | missense variant | C/A;T | snv | 2.8E-05 | 1 | ||
| rs199473327 | 1.000 | 0.120 | 3 | 38550634 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
| rs199473326 | 1.000 | 0.120 | 3 | 38550646 | missense variant | T/C | snv | 1 | |||
| rs150264233 | 1.000 | 0.120 | 3 | 38550661 | stop gained | G/A;T | snv | 1.3E-04 | 3.9E-04 | 1 | |
| rs199473325 | 1.000 | 0.120 | 3 | 38550671 | stop gained | C/A;G;T | snv | 3.2E-05; 2.0E-05 | 1 | ||
| rs45465995 | 1.000 | 0.120 | 3 | 38550683 | missense variant | G/A | snv | 7.6E-05; 8.0E-06 | 9.1E-05 | 1 | |
| rs794728898 | 0.925 | 0.120 | 3 | 38550826 | missense variant | T/C | snv | 1 | |||
| rs199473321 | 0.925 | 0.120 | 3 | 38550856 | missense variant | T/C | snv | 1 | |||
| rs137854610 | 0.925 | 0.120 | 3 | 38550895 | missense variant | C/T | snv | 2.8E-05 | 1.7E-04 | 1 | |
| rs79299226 | 0.851 | 0.120 | 3 | 38550898 | missense variant | A/G | snv | 1 | |||
| rs137854619 | 0.925 | 0.120 | 3 | 38550917 | missense variant | C/T | snv | 2.7E-04 | 7.7E-05 | 1 | |
| rs137854614 | 0.882 | 0.120 | 3 | 38550988 | missense variant | T/C | snv | 1 | |||
| rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 1 | |||
| rs199473317 | 0.882 | 0.120 | 3 | 38551003 | missense variant | T/C | snv | 1 | |||
| rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 2 | ||
| rs199473634 | 0.925 | 0.120 | 3 | 38551036 | missense variant | G/A | snv | 4.0E-05 | 7.7E-05 | 2 | |
| rs199473314 | 1.000 | 0.120 | 3 | 38551043 | missense variant | C/T | snv | 1.6E-05 | 2.1E-05 | 1 | |
| rs199473311 | 0.882 | 0.120 | 3 | 38551070 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs199473632 | 1.000 | 0.120 | 3 | 38551072 | missense variant | T/C | snv | 1 | |||
| rs199473310 | 1.000 | 0.120 | 3 | 38551076 | missense variant | T/A;C;G | snv | 1 | |||
| rs199473631 | 0.925 | 0.120 | 3 | 38551085 | missense variant | C/T | snv | 1 |