| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs5031002 | 1.000 | 0.040 | X | 67722783 | intron variant | G/A | snv | 1.5E-02 | 1.5E-02 | 3 | |
| rs5919393 | 1.000 | 0.080 | X | 67605515 | intron variant | C/T | snv | 0.64 | 1 | ||
| rs1337080 | 1.000 | 0.080 | X | 67659077 | intron variant | G/A | snv | 1 | |||
| rs2255702 | 1.000 | 0.080 | X | 67578269 | intron variant | C/T | snv | 0.36 | 1 | ||
| rs1204038 | 0.882 | 0.160 | X | 67568383 | intron variant | G/A | snv | 0.36 | 1 | ||
| rs4827545 | 1.000 | 0.080 | X | 67608543 | intron variant | A/G;T | snv | 1 | |||
| rs12396249 | 1.000 | 0.080 | X | 67557224 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs6624304 | 0.882 | 0.160 | X | 67655914 | intron variant | T/A;C | snv | 1 | |||
| rs5918760 | 1.000 | 0.080 | X | 67618909 | intron variant | T/A;C | snv | 1 | |||
| rs5918762 | 1.000 | 0.080 | X | 67694959 | 3 prime UTR variant | T/C | snv | 0.64 | 1 | ||
| rs5918764 | 1.000 | 0.080 | X | 67717865 | intron variant | A/G;T | snv | 1 | |||
| rs5918757 | 1.000 | 0.080 | X | 67586188 | intron variant | G/A | snv | 1 |