| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs120074196 | 0.882 | 0.120 | 11 | 2572057 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
| rs199472696 | 0.851 | 0.120 | 11 | 2570670 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 4 | |
| rs199472755 | 0.851 | 0.120 | 11 | 2583478 | missense variant | C/A;G;T | snv | 4.0E-06 | 4 | ||
| rs199472815 | 0.851 | 0.120 | 11 | 2778024 | missense variant | G/A;C | snv | 2.0E-05 | 4 | ||
| rs199473401 | 0.925 | 0.120 | 11 | 2570722 | missense variant | T/C | snv | 4 | |||
| rs397508118 | 0.851 | 0.120 | 11 | 2570720 | frameshift variant | GCGCT/- | delins | 1.4E-05 | 4 | ||
| rs120074179 | 0.925 | 0.120 | 11 | 2572089 | missense variant | G/A;C;T | snv | 3 | |||
| rs120074185 | 0.925 | 0.120 | 11 | 2776032 | missense variant | C/A;T | snv | 1.1E-05; 1.1E-05 | 3 | ||
| rs120074187 | 0.882 | 0.120 | 11 | 2572963 | missense variant | G/A | snv | 4.8E-05 | 2.1E-05 | 3 | |
| rs120074190 | 0.882 | 0.120 | 11 | 2778009 | missense variant | G/A | snv | 4.8E-05 | 5.6E-05 | 3 | |
| rs1554920808 | 1.000 | 0.120 | 11 | 2776991 | missense variant | A/G | snv | 3 | |||
| rs1800171 | 0.882 | 0.120 | 11 | 2583545 | splice region variant | G/A;C;T | snv | 4.0E-06 | 3 | ||
| rs199472678 | 0.925 | 0.120 | 11 | 2445430 | missense variant | A/G | snv | 8.9E-06 | 3 | ||
| rs199472702 | 0.882 | 0.120 | 11 | 2570754 | missense variant | G/A;C | snv | 8.1E-06 | 3 | ||
| rs199472706 | 0.925 | 0.120 | 11 | 2571391 | missense variant | C/T | snv | 4.0E-06 | 1.0E-04 | 3 | |
| rs199472712 | 0.882 | 0.120 | 11 | 2572053 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
| rs199472719 | 0.882 | 0.120 | 11 | 2572104 | missense variant | C/T | snv | 4.1E-06 | 3 | ||
| rs199472720 | 0.925 | 0.120 | 11 | 2572105 | missense variant | G/A;T | snv | 1.6E-05 | 3 | ||
| rs199472756 | 0.925 | 0.120 | 11 | 2583486 | missense variant | G/A | snv | 3 | |||
| rs199472776 | 0.882 | 0.120 | 11 | 2587630 | missense variant | C/G;T | snv | 4.0E-06; 2.0E-04 | 3 | ||
| rs199473411 | 0.882 | 0.120 | 11 | 2585275 | missense variant | C/A;T | snv | 3 | |||
| rs199473442 | 1.000 | 0.120 | 11 | 2445103 | missense variant | C/G;T | snv | 3 | |||
| rs199473456 | 0.882 | 0.120 | 11 | 2571394 | missense variant | C/T | snv | 1.2E-05 | 3 | ||
| rs199473466 | 0.882 | 0.120 | 11 | 2572975 | missense variant | T/C | snv | 3 | |||
| rs397508111 | 0.882 | 0.120 | 11 | 2528023 | splice region variant | G/A;C | snv | 1.2E-05 | 3 |