| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs140516819 | 7 | 55172999 | missense variant | A/C;G | snv | 4.0E-05 | 2.4E-04 | 4 | |||
| rs35918369 | 7 | 55205613 | missense variant | C/T | snv | 3.1E-04 | 3.3E-04 | 4 | |||
| rs961150162 | 7 | 55198779 | missense variant | G/A;C | snv | 3 | |||||
| rs556324078 | 7 | 55205514 | missense variant | T/C | snv | 4.0E-06 | 3 | ||||
| rs746763556 | 7 | 55160230 | missense variant | T/A;G | snv | 1.6E-05; 4.0E-06 | 2 | ||||
| rs987532315 | 7 | 55201782 | splice region variant | G/A | snv | 4.0E-06 | 2 | ||||
| rs1219568637 | 7 | 55143404 | missense variant | G/A | snv | 7.0E-06 | 2 | ||||
| rs723526 | 1.000 | 7 | 55067126 | intron variant | A/G | snv | 0.86 | 2 | |||
| rs1330512770 | 7 | 55161592 | missense variant | G/A | snv | 1.2E-05 | 2 | ||||
| rs150423237 | 7 | 55173087 | missense variant | G/A | snv | 2.1E-04 | 2.4E-04 | 1 | |||
| rs7795743 | 7 | 55182437 | non coding transcript exon variant | G/A | snv | 0.56 | 1 | ||||
| rs483352807 | 7 | 55181402 | missense variant | T/A | snv | 1 | |||||
| rs765091640 | 7 | 55160165 | missense variant | G/A | snv | 1.2E-05 | 1 | ||||
| rs377567759 | 7 | 55160191 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |||
| rs866211550 | 7 | 55160247 | missense variant | G/T | snv | 1 | |||||
| rs774905136 | 7 | 55156555 | synonymous variant | T/C | snv | 5.6E-05 | 1.4E-05 | 1 | |||
| rs587777940 | 7 | 55202667 | missense variant | T/G | snv | 7.0E-06 | 1 | ||||
| rs149248025 | 1.000 | 7 | 55201237 | missense variant | G/A;T | snv | 8.0E-05; 8.0E-06 | 1 | |||
| rs201498575 | 7 | 55165359 | missense variant | G/A | snv | 4.0E-06 | 1 | ||||
| rs759106015 | 7 | 55152588 | missense variant | G/A | snv | 3.2E-05 | 1.4E-05 | 1 | |||
| rs767505234 | 1.000 | 0.040 | 7 | 55174033 | missense variant | C/T | snv | 1.4E-05 | 3 | ||
| rs9642393 | 0.925 | 0.040 | 7 | 55177954 | intron variant | T/C | snv | 0.24 | 2 | ||
| rs4947492 | 0.925 | 0.040 | 7 | 55120299 | intron variant | G/A | snv | 0.50 | 2 | ||
| rs11979158 | 0.882 | 0.040 | 7 | 55091656 | intron variant | A/G;T | snv | 0.20 | 2 | ||
| rs1057519830 | 1.000 | 0.040 | 7 | 55163737 | missense variant | C/T | snv | 2 |