| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121964856 | 0.807 | 0.120 | 1 | 201365297 | missense variant | C/A;T | snv | 8 | |||
| rs45586240 | 0.827 | 0.080 | 1 | 201361989 | missense variant | G/A;T | snv | 4.0E-06 | 7 | ||
| rs121964858 | 0.807 | 0.120 | 1 | 201365244 | missense variant | A/C;G;T | snv | 6 | |||
| rs74315379 | 0.827 | 0.080 | 1 | 201364336 | missense variant | G/A;T | snv | 1.2E-04 | 6 | ||
| rs397516456 | 0.827 | 0.080 | 1 | 201365298 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 5 | |
| rs727504246 | 0.827 | 0.080 | 1 | 201363330 | missense variant | G/A | snv | 5 | |||
| rs727504247 | 0.827 | 0.080 | 1 | 201359217 | stop gained | C/A;T | snv | 4.1E-06 | 7.0E-06 | 5 | |
| rs121964855 | 0.851 | 0.080 | 1 | 201365638 | missense variant | A/T | snv | 4.0E-06 | 4 | ||
| rs121964857 | 0.851 | 0.080 | 1 | 201359245 | missense variant | G/A | snv | 3.6E-04 | 4.3E-04 | 4 | |
| rs200754249 | 0.851 | 0.080 | 1 | 201368212 | missense variant | G/A;T | snv | 4.5E-04; 4.0E-06 | 4 | ||
| rs397516455 | 0.851 | 0.080 | 1 | 201365617 | missense variant | T/G | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs397516457 | 0.851 | 0.080 | 1 | 201365291 | missense variant | C/A;T | snv | 4 | |||
| rs397516463 | 0.851 | 0.080 | 1 | 201364369 | missense variant | G/A | snv | 1.4E-05 | 4 | ||
| rs397516470 | 0.851 | 0.080 | 1 | 201363377 | inframe deletion | CTC/- | delins | 4 | |||
| rs730881116 | 0.851 | 0.080 | 1 | 201359216 | stop gained | C/T | snv | 4 | |||
| rs111377893 | 0.925 | 0.080 | 1 | 201359622 | splice donor variant | C/A;G;T | snv | 2 |