| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267606621 | 0.882 | 0.080 | 16 | 70268356 | missense variant | C/T | snv | 3 | |||
| rs777601008 | 1.000 | 0.080 | 16 | 70268366 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs137852973 | 0.752 | 0.200 | 11 | 62702493 | missense variant | G/A;C | snv | 7.0E-06 | 13 | ||
| rs137852972 | 0.752 | 0.240 | 11 | 62702499 | missense variant | T/C | snv | 1.6E-05 | 10 | ||
| rs748287282 | 1.000 | 0.080 | 11 | 62702475 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs137852643 | 0.925 | 0.080 | 7 | 30609729 | missense variant | G/C | snv | 4.0E-06 | 3 | ||
| rs1554337974 | 0.882 | 0.080 | 7 | 30609643 | missense variant | C/T | snv | 3 | |||
| rs1060502838 | 0.925 | 0.080 | 7 | 30621448 | missense variant | A/G | snv | 2 | |||
| rs1554338260 | 0.925 | 0.080 | 7 | 30612214 | missense variant | A/T | snv | 2 | |||
| rs1060502839 | 1.000 | 0.080 | 7 | 30628565 | missense variant | G/A | snv | 1 | |||
| rs1064795123 | 1.000 | 0.080 | 7 | 30609724 | missense variant | T/C;G | snv | 1 | |||
| rs1554338262 | 1.000 | 0.080 | 7 | 30612215 | missense variant | T/A | snv | 1 | |||
| rs137852975 | 0.851 | 0.240 | 11 | 62692671 | stop gained | C/A | snv | 2.0E-05 | 1.4E-05 | 5 | |
| rs587777606 | 0.851 | 0.160 | 11 | 62691300 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 6 | |
| rs1554982914 | 1.000 | 0.080 | 11 | 62690831 | frameshift variant | CT/- | delins | 1 | |||
| rs1350009895 | 1.000 | 0.080 | 5 | 54456141 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs11575937 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 29 | |||
| rs386134243 | 0.708 | 0.360 | 1 | 156135967 | missense variant | C/A;T | snv | 4.0E-06 | 16 | ||
| rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
| rs61672878 | 0.776 | 0.200 | 1 | 156136094 | missense variant | G/A;T | snv | 11 | |||
| rs57520892 | 0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 | 8 | ||
| rs58932704 | 0.776 | 0.200 | 1 | 156136413 | missense variant | C/T | snv | 8 | |||
| rs150840924 | 0.807 | 0.240 | 1 | 156136359 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 7 | |
| rs58596362 | 0.827 | 0.280 | 1 | 156138613 | splice region variant | C/A;T | snv | 8.1E-06 | 7 | ||
| rs59026483 | 0.827 | 0.160 | 1 | 156134457 | missense variant | C/T | snv | 7.0E-06 | 7 |