| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11574311 | 0.776 | 0.160 | 8 | 31119144 | intron variant | T/C | snv | 0.16 | 8 | ||
| rs2725338 | 0.790 | 0.120 | 8 | 31042501 | intron variant | G/A | snv | 7.6E-02 | 7 | ||
| rs1063147 | 0.807 | 0.120 | 15 | 90811275 | synonymous variant | C/T | snv | 0.15 | 6 | ||
| rs2725383 | 0.807 | 0.120 | 8 | 31075099 | intron variant | C/G | snv | 0.76 | 6 | ||
| rs4733220 | 0.807 | 0.120 | 8 | 31043374 | intron variant | A/G | snv | 0.50 | 6 | ||
| rs104893736 | 0.827 | 0.040 | 3 | 186539566 | missense variant | C/A | snv | 5 | |||
| rs9640883 | 0.882 | 0.120 | 7 | 134431881 | intron variant | G/A | snv | 0.21 | 4 | ||
| rs6657114 | 0.925 | 0.120 | 1 | 147905591 | upstream gene variant | G/T | snv | 0.27 | 2 | ||
| rs7541950 | 0.925 | 0.120 | 1 | 147903855 | upstream gene variant | C/T | snv | 0.55 | 2 | ||
| rs2132397 | 0.925 | 0.120 | 1 | 147909431 | downstream gene variant | A/G | snv | 0.17 | 2 | ||
| rs2096488 | 1.000 | 0.040 | 21 | 25971876 | intron variant | A/C | snv | 0.17 | 1 | ||
| rs13155993 | 1.000 | 0.040 | 5 | 11108043 | intron variant | C/T | snv | 7.0E-02 | 1 | ||
| rs13170756 | 1.000 | 0.040 | 5 | 11110237 | intron variant | C/A;T | snv | 1 | |||
| rs17183619 | 1.000 | 0.040 | 5 | 11111141 | intron variant | T/G | snv | 7.6E-02 | 1 | ||
| rs6678616 | 1.000 | 0.040 | 1 | 16148628 | synonymous variant | C/G;T | snv | 0.30 | 1 |