| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs775040765 | 1.000 | 7 | 140800366 | missense variant | T/C | snv | 8.0E-05 | 1.4E-05 | 2 | ||
| rs121913335 | 7 | 140753375 | missense variant | T/G | snv | 1 | |||||
| rs121913336 | 7 | 140753374 | missense variant | G/C;T | snv | 1 | |||||
| rs121913362 | 7 | 140753359 | missense variant | T/C | snv | 1 | |||||
| rs1325951163 | 1.000 | 7 | 140801517 | missense variant | C/G;T | snv | 4.0E-06 | 1 | |||
| rs1562957000 | 1.000 | 7 | 140781621 | missense variant | T/C | snv | 1 | ||||
| rs867748453 | 7 | 140781608 | missense variant | G/A | snv | 1 | |||||
| rs121913371 | 1.000 | 0.040 | 7 | 140781678 | missense variant | G/A;T | snv | 4.0E-06; 8.0E-06 | 3 | ||
| rs397507482 | 0.882 | 0.040 | 7 | 140753386 | missense variant | A/C | snv | 3 | |||
| rs121913368 | 0.925 | 0.040 | 7 | 140753345 | missense variant | AG/GA | mnv | 2 | |||
| rs121913225 | 1.000 | 0.040 | 7 | 140753351 | missense variant | A/G | snv | 1 | |||
| rs121913226 | 1.000 | 0.040 | 7 | 140753332 | inframe deletion | TTT/- | del | 1 | |||
| rs121913363 | 1.000 | 0.040 | 7 | 140753361 | missense variant | T/C | snv | 1 | |||
| rs121913372 | 1.000 | 0.040 | 7 | 140753321 | missense variant | CT/AA | mnv | 1 | |||
| rs121913373 | 1.000 | 0.040 | 7 | 140753321 | missense variant | C/T | snv | 1 | |||
| rs1639679 | 1.000 | 0.040 | 7 | 140778454 | intron variant | G/T | snv | 9.8E-02 | 1 | ||
| rs1057519720 | 0.851 | 0.080 | 7 | 140781602 | missense variant | CC/AA;GA | mnv | 4 | |||
| rs727502902 | 0.882 | 0.080 | 7 | 140753338 | inframe insertion | -/TAG | delins | 4.0E-06 | 4 | ||
| rs114729114 | 0.925 | 0.080 | 7 | 140910797 | intron variant | C/T | snv | 1.1E-02 | 3 | ||
| rs868021367 | 0.882 | 0.080 | 7 | 140753319 | missense variant | C/G | snv | 3 | |||
| rs1057519719 | 1.000 | 0.080 | 7 | 140781593 | missense variant | T/C | snv | 2 | |||
| rs11762469 | 1.000 | 0.080 | 7 | 140914412 | intron variant | A/G;T | snv | 2 | |||
| rs121913376 | 0.925 | 0.080 | 7 | 140781597 | missense variant | C/A;T | snv | 2 | |||
| rs1238788540 | 0.925 | 0.080 | 7 | 140800368 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs730880413 | 0.925 | 0.080 | 7 | 140801460 | missense variant | C/T | snv | 4.0E-06 | 2 |