| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1805127 | 0.732 | 0.240 | 21 | 34449523 | missense variant | T/C | snv | 0.64 | 2.0E-04 | 17 | |
| rs1805128 | 0.776 | 0.160 | 21 | 34449382 | missense variant | C/T | snv | 9.4E-03 | 10 | ||
| rs121912504 | 0.851 | 0.200 | 7 | 150951711 | missense variant | G/A | snv | 6 | |||
| rs199472910 | 0.827 | 0.120 | 7 | 150952508 | missense variant | G/A | snv | 1.2E-05 | 5 | ||
| rs199472921 | 0.882 | 0.120 | 7 | 150951712 | missense variant | C/G;T | snv | 5 | |||
| rs199472936 | 0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv | 5 | |||
| rs28928905 | 0.851 | 0.120 | 7 | 150952514 | missense variant | C/G;T | snv | 5 | |||
| rs121912507 | 0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv | 4 | |||
| rs199473039 | 0.851 | 0.120 | 7 | 150951512 | missense variant | G/A;C;T | snv | 9.5E-05 | 4 | ||
| rs199473428 | 0.851 | 0.120 | 7 | 150951643 | missense variant | C/A;G;T | snv | 8.0E-06 | 4 | ||
| rs121912512 | 0.882 | 0.120 | 7 | 150950311 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs1800171 | 0.882 | 0.120 | 11 | 2583545 | splice region variant | G/A;C;T | snv | 4.0E-06 | 3 | ||
| rs189014161 | 0.882 | 0.120 | 7 | 150950336 | stop gained | G/A;C;T | snv | 1.6E-05; 4.0E-06 | 3 | ||
| rs199472842 | 0.925 | 0.120 | 7 | 150974861 | missense variant | C/G;T | snv | 3 | |||
| rs199472918 | 0.882 | 0.120 | 7 | 150951738 | missense variant | A/G | snv | 7.2E-05 | 5.6E-05 | 3 | |
| rs199472944 | 0.882 | 0.120 | 7 | 150951552 | missense variant | G/A | snv | 3 | |||
| rs199472957 | 0.882 | 0.120 | 7 | 150951507 | missense variant | T/A;C;G | snv | 3 | |||
| rs199472968 | 0.925 | 0.120 | 7 | 150951484 | missense variant | C/T | snv | 3 | |||
| rs199472990 | 0.882 | 0.120 | 7 | 150950312 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs199473522 | 0.882 | 0.120 | 7 | 150951583 | missense variant | C/T | snv | 3 | |||
| rs199473538 | 0.882 | 0.120 | 7 | 150948981 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs36210422 | 0.882 | 0.120 | 7 | 150958449 | missense variant | G/A;C | snv | 3.2E-04 | 3 | ||
| rs762510312 | 0.925 | 0.120 | 7 | 150946956 | missense variant | G/A;C | snv | 4.8E-05; 1.2E-05 | 3 | ||
| rs794728455 | 0.882 | 0.120 | 7 | 150947796 | frameshift variant | C/-;CC | delins | 2.4E-05 | 3 | ||
| rs9333649 | 0.882 | 0.200 | 7 | 150951679 | missense variant | C/A;G;T | snv | 3 |