| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs752742313 | 0.637 | 0.320 | 3 | 138655502 | missense variant | C/T | snv | 1.2E-05 | 36 | ||
| rs752021744 | 0.689 | 0.440 | 3 | 138759306 | missense variant | T/C | snv | 1.2E-05 | 29 | ||
| rs361072 | 0.882 | 0.120 | 3 | 138759702 | intron variant | G/A;C | snv | 4 | |||
| rs773297988 | 0.882 | 0.080 | 3 | 138698965 | missense variant | T/C | snv | 4.0E-06 | 3.5E-05 | 4 | |
| rs1235228469 | 0.925 | 0.120 | 3 | 138684714 | missense variant | C/A | snv | 8.0E-06 | 2 | ||
| rs149005978 | 3 | 138783216 | intron variant | T/C | snv | 1.4E-02 | 2 | ||||
| rs371428527 | 0.925 | 3 | 138737869 | missense variant | T/C;G | snv | 1.2E-05 | 1.4E-05 | 2 | ||
| rs1171134914 | 3 | 138655454 | missense variant | T/C | snv | 1 | |||||
| rs1174984399 | 1.000 | 0.120 | 3 | 138714505 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1233960622 | 1.000 | 0.080 | 3 | 138699044 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs1304149814 | 3 | 138699042 | missense variant | A/C | snv | 4.0E-06 | 1 | ||||
| rs1331108652 | 3 | 138694820 | stop gained | G/A | snv | 4.0E-06 | 1 | ||||
| rs754551112 | 1.000 | 0.080 | 3 | 138737810 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |