| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61749414 | 0.882 | 0.080 | 1 | 94062611 | stop gained | G/A;T | snv | 2 | |||
| rs61749409 | 0.882 | 0.080 | 1 | 94062710 | missense variant | G/A | snv | 4.4E-05 | 2.1E-05 | 2 | |
| rs61751392 | 0.827 | 0.080 | 1 | 94063250 | missense variant | A/G | snv | 1.5E-04 | 1.7E-04 | 1 | |
| rs3112831 | 1.000 | 0.080 | 1 | 94078678 | missense variant | T/C;G | snv | 0.26 | 0.26 | 2 | |
| rs794727903 | 0.925 | 0.080 | 1 | 94080697 | stop gained | G/A | snv | 2 | |||
| rs781716640 | 1.000 | 1 | 94080709 | missense variant | G/A | snv | 2.0E-05 | 1.4E-05 | 1 | ||
| rs560426 | 0.851 | 0.200 | 1 | 94087882 | intron variant | C/T | snv | 0.53 | 5 | ||
| rs62645944 | 0.807 | 0.080 | 1 | 94098794 | splice region variant | C/A | snv | 8.8E-05 | 6.3E-05 | 3 | |
| rs61748537 | 0.882 | 0.160 | 1 | 94098906 | missense variant | C/G;T | snv | 4.0E-05; 8.0E-06 | 2 | ||
| rs61750200 | 0.790 | 0.080 | 1 | 94098928 | missense variant | G/A;T | snv | 1.1E-04; 8.0E-06 | 4 | ||
| rs481931 | 0.882 | 0.120 | 1 | 94104460 | intron variant | G/T | snv | 0.32 | 1 | ||
| rs886044720 | 0.925 | 0.080 | 1 | 94112973 | missense variant | A/C | snv | 1 | |||
| rs121909205 | 1.000 | 1 | 94120994 | missense variant | G/A;T | snv | 1.6E-05; 3.6E-05 | 1 |