| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 4 | ||
| rs199473072 | 0.827 | 0.160 | 3 | 38613773 | missense variant | G/A | snv | 1.2E-05 | 8.4E-05 | 3 | |
| rs199473282 | 0.827 | 0.120 | 3 | 38551513 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
| rs137854606 | 0.882 | 0.120 | 3 | 38604062 | missense variant | C/A | snv | 2 | |||
| rs199473062 | 0.827 | 0.120 | 3 | 38622401 | stop gained | C/A;G;T | snv | 4.1E-06 | 2 | ||
| rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 2 | |
| rs199473153 | 0.882 | 0.120 | 3 | 38597737 | stop gained | C/A;T | snv | 4.0E-06 | 2 | ||
| rs199473207 | 0.882 | 0.120 | 3 | 38566555 | missense variant | G/A | snv | 2 | |||
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 2 | ||
| rs137854607 | 0.882 | 0.120 | 3 | 38554309 | missense variant | C/G;T | snv | 1 | |||
| rs137854608 | 0.925 | 0.120 | 3 | 38609776 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 1 | |
| rs199473118 | 1.000 | 0.080 | 3 | 38604067 | missense variant | G/A | snv | 4.4E-06 | 1 |