| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs199473035 | 1.000 | 0.120 | 7 | 150945388 | missense variant | G/A | snv | 4.8E-05 | 2.1E-05 | 1 | |
| rs199473546 | 1.000 | 0.120 | 7 | 150945502 | missense variant | T/C | snv | 1.4E-05 | 1 | ||
| rs199473545 | 1.000 | 0.120 | 7 | 150946929 | missense variant | G/A;C | snv | 3.3E-05; 4.1E-06 | 1 | ||
| rs199473029 | 1.000 | 0.120 | 7 | 150946974 | missense variant | T/C | snv | 4.0E-06 | 2.1E-05 | 1 | |
| rs199473027 | 1.000 | 0.120 | 7 | 150947011 | missense variant | G/C | snv | 1 | |||
| rs199473026 | 1.000 | 0.120 | 7 | 150947334 | missense variant | A/G | snv | 1 | |||
| rs199473544 | 1.000 | 0.120 | 7 | 150947368 | missense variant | C/A;T | snv | 2.8E-05; 1.2E-04 | 1 | ||
| rs199473022 | 1.000 | 0.120 | 7 | 150947373 | missense variant | C/T | snv | 6.9E-05 | 1.3E-04 | 1 | |
| rs199473021 | 1.000 | 0.120 | 7 | 150947383 | missense variant | G/A;T | snv | 1.3E-04; 6.9E-06 | 1 | ||
| rs199473542 | 1.000 | 0.120 | 7 | 150947460 | missense variant | C/A;T | snv | 1.7E-05 | 1 | ||
| rs199473019 | 1.000 | 0.120 | 7 | 150947466 | missense variant | C/T | snv | 5.5E-06 | 1.4E-05 | 1 | |
| rs199473018 | 1.000 | 0.120 | 7 | 150947493 | missense variant | T/A | snv | 1 | |||
| rs149955375 | 1.000 | 0.120 | 7 | 150947623 | missense variant | G/A | snv | 1.3E-04 | 2.2E-04 | 1 | |
| rs199473017 | 1.000 | 0.120 | 7 | 150947668 | missense variant | G/A | snv | 3.4E-05 | 2.1E-05 | 1 | |
| rs121912514 | 0.925 | 0.120 | 7 | 150947729 | missense variant | G/A;T | snv | 6.0E-05; 6.0E-06 | 1 | ||
| rs199473540 | 1.000 | 0.120 | 7 | 150947761 | missense variant | C/T | snv | 5.0E-05 | 4.2E-05 | 1 | |
| rs199473010 | 1.000 | 0.120 | 7 | 150947798 | missense variant | C/T | snv | 1 | |||
| rs199473009 | 1.000 | 0.120 | 7 | 150947800 | missense variant | C/A;G;T | snv | 7.9E-06; 3.9E-05; 7.1E-05 | 1 | ||
| rs199473439 | 1.000 | 0.120 | 7 | 150947806 | missense variant | C/A;T | snv | 3.9E-05 | 1 | ||
| rs199473440 | 1.000 | 0.120 | 7 | 150947807 | missense variant | G/A | snv | 2.4E-05 | 1.4E-05 | 1 | |
| rs199473670 | 1.000 | 0.120 | 7 | 150947812 | missense variant | C/T | snv | 4.0E-05 | 2.1E-05 | 1 | |
| rs199473438 | 1.000 | 0.120 | 7 | 150947813 | missense variant | G/A;C | snv | 8.0E-06; 1.6E-05 | 1 | ||
| rs76420733 | 1.000 | 0.120 | 7 | 150947821 | missense variant | G/A | snv | 5.7E-05 | 4.9E-05 | 1 | |
| rs77331749 | 0.925 | 0.120 | 7 | 150947833 | missense variant | G/A | snv | 4.0E-04 | 5.5E-04 | 1 | |
| rs199473435 | 1.000 | 0.120 | 7 | 150947854 | missense variant | G/A | snv | 7.2E-05 | 4.2E-05 | 1 |