| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1373692 | 1.000 | 0.040 | 5 | 40431081 | non coding transcript exon variant | A/C;T | snv | 1 | |||
| rs140068907 | 1.000 | 0.040 | 6 | 32691666 | regulatory region variant | A/C | snv | 3.4E-03 | 1 | ||
| rs147629807 | 1.000 | 0.040 | 5 | 108553338 | intergenic variant | T/- | del | 1 | |||
| rs1487630 | 1.000 | 0.040 | 4 | 38334202 | intergenic variant | C/T | snv | 0.14 | 1 | ||
| rs1495465 | 1.000 | 0.040 | 14 | 57549696 | intergenic variant | C/A | snv | 7.0E-06 | 1 | ||
| rs1499555 | 1.000 | 0.040 | 9 | 22589172 | intergenic variant | G/A | snv | 0.36 | 1 | ||
| rs184950714 | 1.000 | 0.040 | 6 | 32668951 | upstream gene variant | G/A | snv | 5.6E-02 | 1 | ||
| rs1858074 | 1.000 | 0.040 | 5 | 132036306 | intergenic variant | A/G | snv | 0.22 | 1 | ||
| rs1992660 | 1.000 | 0.040 | 5 | 40414965 | upstream gene variant | C/T | snv | 0.58 | 1 | ||
| rs1992662 | 1.000 | 0.040 | 5 | 40393750 | intergenic variant | A/G | snv | 0.29 | 1 | ||
| rs224090 | 1.000 | 0.040 | 10 | 62781559 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs224143 | 1.000 | 0.040 | 10 | 62718076 | intron variant | G/A | snv | 0.64 | 1 | ||
| rs226534 | 1.000 | 0.040 | X | 127768516 | intergenic variant | A/G | snv | 0.34 | 1 | ||
| rs2361755 | 1.000 | 0.040 | 16 | 85976080 | intron variant | G/C;T | snv | 1 | |||
| rs247660 | 1.000 | 0.040 | 5 | 85462322 | upstream gene variant | A/C | snv | 0.21 | 1 | ||
| rs255969 | 1.000 | 0.040 | 5 | 95314200 | intergenic variant | C/T | snv | 0.85 | 1 | ||
| rs2858332 | 1.000 | 0.040 | 6 | 32713384 | upstream gene variant | G/T | snv | 0.54 | 1 | ||
| rs2927488 | 1.000 | 0.040 | 19 | 44728212 | upstream gene variant | G/A | snv | 0.22 | 1 | ||
| rs3091338 | 1.000 | 0.040 | 5 | 132067045 | downstream gene variant | C/T | snv | 0.30 | 1 | ||
| rs3897478 | 1.000 | 0.040 | 1 | 119908567 | downstream gene variant | T/C | snv | 0.17 | 1 | ||
| rs3916442 | 1.000 | 0.040 | 5 | 132033475 | intergenic variant | G/A | snv | 0.53 | 1 | ||
| rs394522 | 1.000 | 0.040 | 6 | 166984583 | intron variant | A/C;G | snv | 1 | |||
| rs415890 | 1.000 | 0.040 | 6 | 166993145 | intron variant | G/A;C | snv | 1 | |||
| rs4820425 | 1.000 | 0.040 | 22 | 41035338 | intergenic variant | C/A;G;T | snv | 1 | |||
| rs495662 | 1.000 | 0.040 | 6 | 117802987 | intergenic variant | G/A | snv | 0.92 | 1 |