| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918010 | 0.827 | 0.200 | 1 | 21573781 | missense variant | T/C | snv | 7.2E-05 | 4.2E-05 | 5 | |
| rs121918013 | 0.827 | 0.120 | 1 | 21563158 | missense variant | G/A | snv | 5 | |||
| rs121918014 | 0.827 | 0.120 | 1 | 21576582 | missense variant | A/G | snv | 2.0E-05 | 5.6E-05 | 5 | |
| rs121918002 | 0.851 | 0.080 | 1 | 21573683 | missense variant | A/C | snv | 3.6E-05 | 7.0E-05 | 4 | |
| rs121918007 | 0.851 | 0.080 | 1 | 21564139 | missense variant | G/A;C | snv | 2.4E-03; 4.0E-06 | 4 | ||
| rs121918008 | 0.851 | 0.080 | 1 | 21575868 | missense variant | A/T | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs121918009 | 0.851 | 0.080 | 1 | 21575736 | missense variant | G/A | snv | 4 | |||
| rs121918011 | 0.851 | 0.080 | 1 | 21563219 | missense variant | G/A;C | snv | 1.4E-04 | 4 | ||
| rs138690664 | 0.851 | 0.120 | 1 | 21577421 | missense variant | C/G;T | snv | 1.6E-05 | 3.5E-05 | 4 | |
| rs149889416 | 0.882 | 0.160 | 1 | 21577436 | missense variant | G/A | snv | 4.5E-05 | 3.5E-05 | 3 | |
| rs771540767 | 0.882 | 0.080 | 1 | 21575879 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs781272386 | 0.882 | 0.080 | 1 | 21570327 | missense variant | G/A;C;T | snv | 8.0E-06; 4.0E-06; 8.0E-06 | 3 | ||
| rs1054159992 | 0.925 | 0.080 | 1 | 21577448 | missense variant | G/A;T | snv | 7.0E-06 | 2 | ||
| rs387906525 | 0.925 | 0.080 | 1 | 21577632 | frameshift variant | T/- | del | 8.7E-06; 1.3E-05 | 2 | ||
| rs751404811 | 0.925 | 0.080 | 1 | 21575901 | frameshift variant | C/-;CC | delins | 2.4E-05 | 2 |