Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs66469337 | 1.000 | 0.120 | X | 38421050 | missense variant | T/C;G | snv | 1 | |||
| rs66539573 | 1.000 | 0.120 | X | 38381393 | missense variant | A/G;T | snv | 1 | |||
| rs66550389 | 1.000 | 0.120 | X | 38369854 | missense variant | G/A;C;T | snv | 1 | |||
| rs66626662 | 1.000 | 0.120 | X | 38401372 | missense variant | G/A;C | snv | 1 | |||
| rs66642398 | 1.000 | 0.120 | X | 38403663 | missense variant | G/A;T | snv | 1 | |||
| rs66656800 | 1.000 | 0.120 | X | 38381429 | missense variant | G/A;C;T | snv | 1 | |||
| rs66724222 | 1.000 | 0.120 | X | 38408988 | missense variant | G/A;T | snv | 1 | |||
| rs66741318 | 1.000 | 0.120 | X | 38401332 | missense variant | G/C;T | snv | 1 | |||
| rs66867430 | 1.000 | 0.120 | X | 38401391 | missense variant | A/C;G | snv | 1 | |||
| rs67120076 | 1.000 | 0.120 | X | 38408752 | missense variant | C/G;T | snv | 1 | |||
| rs67156896 | 1.000 | 0.120 | X | 38408949 | missense variant | C/A;T | snv | 1 | |||
| rs67294955 | 1.000 | 0.120 | X | 38403660 | missense variant | G/A | snv | 1 | |||
| rs67333670 | 1.000 | 0.120 | X | 38408943 | missense variant | C/A;T | snv | 1 | |||
| rs67468335 | 1.000 | 0.120 | X | 38411901 | missense variant | T/C;G | snv | 1 | |||
| rs67486158 | 1.000 | 0.120 | X | 38367361 | stop gained | G/A;T | snv | 4.9E-05 | 1 | ||
| rs67501347 | 1.000 | 0.120 | X | 38411908 | missense variant | C/A;G | snv | 1 | |||
| rs67870244 | 1.000 | 0.120 | X | 38411900 | missense variant | C/G;T | snv | 5.5E-06 | 1 | ||
| rs67939655 | 1.000 | 0.120 | X | 38367353 | missense variant | A/C;T | snv | 1.6E-04 | 1 | ||
| rs67954347 | 1.000 | 0.120 | X | 38401367 | missense variant | T/A;C;G | snv | 1 | |||
| rs67993095 | 1.000 | 0.120 | X | 38411899 | missense variant | A/G;T | snv | 1 | |||
| rs68026851 | 1.000 | 0.120 | X | 38401310 | missense variant | G/A;C | snv | 1 | |||
| rs68031618 | 1.000 | 0.120 | X | 38352773 | missense variant | G/A;C | snv | 1 | |||
| rs68033093 | 1.000 | 0.120 | X | 38401412 | missense variant | A/G;T | snv | 1 | |||
| rs72554306 | 1.000 | 0.120 | X | 38367328 | missense variant | G/T | snv | 1 | |||
| rs72554307 | 1.000 | 0.120 | X | 38367331 | missense variant | C/T | snv | 1.1E-05 | 1 |