| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs553509 | 0.925 | 0.040 | X | 104013293 | missense variant | T/C | snv | 0.38 | 3 | ||
| rs55763075 | 0.827 | 0.120 | 1 | 11790377 | 3 prime UTR variant | C/T | snv | 2.1E-05 | 6 | ||
| rs6080550 | 0.851 | 0.040 | 20 | 1778944 | intron variant | C/G;T | snv | 9.6E-02 | 5 | ||
| rs6166 | 0.708 | 0.240 | 2 | 48962782 | missense variant | C/T | snv | 0.57 | 0.57 | 17 | |
| rs68073206 | 1.000 | 0.040 | 2 | 48721568 | 3 prime UTR variant | A/C | snv | 0.29 | 2 | ||
| rs7174015 | 0.925 | 0.040 | 15 | 50424871 | intron variant | G/A;T | snv | 3 | |||
| rs724078 | 0.925 | 0.040 | 6 | 29521271 | intergenic variant | G/A | snv | 0.41 | 3 | ||
| rs7867029 | 0.925 | 0.040 | 9 | 78405502 | intergenic variant | G/C | snv | 0.22 | 3 |