| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs193922726 | 1.000 | 0.080 | 3 | 38551188 | missense variant | G/A;C | snv | 6.0E-05 | 1 | ||
| rs199473043 | 1.000 | 0.120 | 3 | 38633282 | missense variant | C/A | snv | 1 | |||
| rs199473045 | 0.925 | 0.120 | 3 | 38633228 | missense variant | C/A;T | snv | 8.0E-06; 2.5E-04 | 2 | ||
| rs199473047 | 1.000 | 0.120 | 3 | 38633180 | missense variant | C/G;T | snv | 4.8E-05 | 1 | ||
| rs199473048 | 1.000 | 0.120 | 3 | 38633166 | missense variant | C/T | snv | 5.3E-05 | 5.6E-05 | 1 | |
| rs199473049 | 1.000 | 0.120 | 3 | 38633150 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs199473050 | 1.000 | 0.080 | 3 | 38633098 | missense variant | A/C | snv | 4.4E-05 | 1.4E-05 | 1 | |
| rs199473051 | 0.925 | 0.120 | 3 | 38633058 | missense variant | C/T | snv | 1 | |||
| rs199473052 | 1.000 | 0.080 | 3 | 38630425 | missense variant | A/G | snv | 1 | |||
| rs199473053 | 1.000 | 0.080 | 3 | 38630422 | missense variant | A/C | snv | 1 | |||
| rs199473054 | 1.000 | 0.080 | 3 | 38630420 | missense variant | C/G;T | snv | 2.0E-05; 2.8E-05 | 1 | ||
| rs199473055 | 0.882 | 0.120 | 3 | 38630393 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
| rs199473056 | 1.000 | 0.080 | 3 | 38630376 | missense variant | G/A;T | snv | 3.6E-05; 4.0E-06 | 1 | ||
| rs199473057 | 1.000 | 0.120 | 3 | 38630360 | missense variant | T/C | snv | 1 | |||
| rs199473058 | 0.925 | 0.080 | 3 | 38630341 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs199473059 | 1.000 | 0.120 | 3 | 38630330 | missense variant | C/G;T | snv | 2.2E-04 | 1 | ||
| rs199473060 | 1.000 | 3 | 38622468 | missense variant | C/T | snv | 4.1E-06 | 7.0E-06 | 1 | ||
| rs199473061 | 1.000 | 0.080 | 3 | 38622446 | missense variant | C/T | snv | 1.2E-04 | 2.1E-05 | 1 | |
| rs199473062 | 0.827 | 0.120 | 3 | 38622401 | stop gained | C/A;G;T | snv | 4.1E-06 | 2 | ||
| rs199473063 | 1.000 | 0.080 | 3 | 38620929 | missense variant | C/G | snv | 1 | |||
| rs199473065 | 1.000 | 0.080 | 3 | 38620921 | missense variant | G/C | snv | 1 | |||
| rs199473066 | 1.000 | 0.080 | 3 | 38620910 | missense variant | A/G | snv | 1 | |||
| rs199473067 | 1.000 | 0.080 | 3 | 38620900 | missense variant | G/A;T | snv | 1.6E-05 | 1 | ||
| rs199473070 | 0.925 | 0.120 | 3 | 38613811 | missense variant | A/G;T | snv | 2 | |||
| rs199473071 | 0.925 | 0.120 | 3 | 38613772 | missense variant | C/T | snv | 1.7E-05 | 1.4E-05 | 1 |