| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1064793575 | 0.925 | 0.040 | X | 136016706 | frameshift variant | GT/- | delins | 6 | |||
| rs1057518789 | 0.925 | 0.040 | 16 | 3728803 | stop gained | G/A | snv | 2 | |||
| rs202193096 | 0.925 | 0.040 | 16 | 30089130 | missense variant | G/A | snv | 2.2E-04 | 1.0E-04 | 2 | |
| rs1057518828 | 1.000 | 0.040 | 17 | 44911317 | missense variant | T/G | snv | 1 | |||
| rs11598177 | 1.000 | 0.040 | 10 | 101220399 | regulatory region variant | T/C | snv | 0.47 | 1 | ||
| rs12432469 | 1.000 | 0.040 | 14 | 26807946 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs12432472 | 1.000 | 0.040 | 14 | 26807959 | intron variant | A/C | snv | 0.25 | 1 | ||
| rs1322330 | 1.000 | 0.040 | 10 | 101231902 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs1322332 | 1.000 | 0.040 | 10 | 101222891 | downstream gene variant | T/C | snv | 0.50 | 1 | ||
| rs1400180 | 1.000 | 0.040 | 3 | 129285 | intron variant | T/G | snv | 0.37 | 1 | ||
| rs1400182 | 1.000 | 0.040 | 3 | 128928 | intron variant | C/G;T | snv | 1 | |||
| rs1407409 | 1.000 | 0.040 | 10 | 101225650 | upstream gene variant | T/C | snv | 0.22 | 1 | ||
| rs1535462 | 1.000 | 0.040 | 10 | 101214115 | TF binding site variant | A/C;G | snv | 1 | |||
| rs1568097 | 1.000 | 0.040 | 3 | 138468 | intron variant | T/C | snv | 0.42 | 1 | ||
| rs1588962 | 1.000 | 0.040 | 3 | 142352 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs17326792 | 1.000 | 0.040 | 3 | 131073 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs1878169 | 1.000 | 0.040 | 3 | 123429 | intron variant | A/T | snv | 0.32 | 1 | ||
| rs200590764 | 1.000 | 0.040 | 10 | 101216904 | intergenic variant | -/T | delins | 6.6E-03 | 1 | ||
| rs2281894 | 1.000 | 0.040 | 1 | 109267922 | synonymous variant | C/A | snv | 0.22 | 0.17 | 1 | |
| rs2393069 | 1.000 | 0.040 | 10 | 56359144 | intron variant | C/G;T | snv | 1 | |||
| rs3950032 | 1.000 | 0.040 | 10 | 101214352 | TF binding site variant | A/C;G;T | snv | 1 | |||
| rs4684051 | 1.000 | 0.040 | 3 | 136842 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs594791 | 1.000 | 0.040 | 10 | 101236039 | intron variant | T/C;G | snv | 1 | |||
| rs751819844 | 1.000 | 0.040 | 7 | 81705724 | missense variant | G/A | snv | 6.4E-05 | 2.8E-05 | 1 | |
| rs76319884 | 1.000 | 0.040 | 10 | 101216249 | intergenic variant | C/G | snv | 8.8E-02 | 1 |