| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs200215055 | 0.742 | 0.400 | 1 | 161626196 | missense variant | C/A;G;T | snv | 1.5E-03; 1.2E-05; 4.0E-06 | 11 | ||
| rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 10 | ||
| rs11209032 | 0.752 | 0.400 | 1 | 67274409 | upstream gene variant | G/A | snv | 0.30 | 10 | ||
| rs1308699981 | 0.807 | 0.440 | 1 | 161543085 | missense variant | G/A | snv | 4.0E-06 | 7 | ||
| rs2297630 | 0.827 | 0.160 | 10 | 44376100 | intron variant | G/A;T | snv | 0.21 | 6 | ||
| rs266085 | 0.851 | 0.200 | 10 | 44378805 | intron variant | C/T | snv | 0.32 | 5 | ||
| rs80338835 | 0.925 | 0.200 | 22 | 36282754 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs1467199 | 1.000 | 0.120 | 2 | 191015776 | intron variant | C/G;T | snv | 2 | |||
| rs146436713 | 1.000 | 0.120 | 17 | 16948957 | missense variant | C/A;T | snv | 8.0E-06; 1.9E-04 | 1 | ||
| rs1161169998 | 1.000 | 0.120 | 13 | 108303360 | missense variant | G/A | snv | 7.0E-06 | 1 |