| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1046276 | 1.000 | 0.040 | 16 | 30903305 | 3 prime UTR variant | T/C | snv | 0.62 | 3 | ||
| rs121918817 | 0.882 | 0.040 | 2 | 166045080 | missense variant | C/T | snv | 1.7E-03 | 1.5E-03 | 3 | |
| rs1570624 | 0.882 | 0.040 | 6 | 52454252 | missense variant | G/A | snv | 1.0E-02 | 9.6E-03 | 3 | |
| rs1805032 | 1.000 | 0.040 | 2 | 151839238 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs765078446 | 0.925 | 0.040 | 6 | 53013900 | missense variant | T/G | snv | 2.0E-05 | 2.1E-05 | 3 | |
| rs10496964 | 0.925 | 0.040 | 2 | 144602342 | intergenic variant | C/T | snv | 0.12 | 2 | ||
| rs12059546 | 0.925 | 0.040 | 1 | 239806797 | intron variant | A/G | snv | 0.30 | 2 | ||
| rs121434579 | 0.925 | 0.040 | 5 | 161895774 | missense variant | C/A | snv | 2 | |||
| rs149055334 | 0.925 | 0.040 | 6 | 52424111 | missense variant | C/A | snv | 1.9E-03 | 7.7E-03 | 2 | |
| rs79761183 | 0.925 | 0.040 | 6 | 52452776 | missense variant | G/A;C | snv | 2.0E-03; 8.0E-06; 1.2E-05 | 7.6E-03 | 2 | |
| rs1376122529 | 1.000 | 0.040 | 2 | 238252912 | splice region variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs137852777 | 1.000 | 0.040 | 6 | 52452742 | missense variant | G/A | snv | 4.8E-05 | 1 | ||
| rs137852778 | 1.000 | 0.040 | 6 | 52454128 | missense variant | G/A;T | snv | 2.0E-05 | 1 | ||
| rs142458862 | 1.000 | 0.040 | 6 | 52492274 | missense variant | T/G | snv | 1.8E-04 | 1.2E-04 | 1 | |
| rs149998588 | 1.000 | 0.040 | 6 | 52479759 | stop gained | C/T | snv | 3.2E-05 | 1.4E-05 | 1 | |
| rs17851770 | 1.000 | 0.040 | 6 | 52492273 | missense variant | A/C | snv | 6.2E-02 | 6.2E-02 | 1 | |
| rs183899632 | 1.000 | 0.040 | 8 | 67746023 | missense variant | C/A;T | snv | 5.6E-05; 4.0E-05 | 1 | ||
| rs200191497 | 1.000 | 0.040 | 6 | 52438562 | missense variant | C/T | snv | 7.2E-05 | 1.4E-05 | 1 | |
| rs2029461 | 1.000 | 0.040 | 6 | 34138013 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs2208592 | 1.000 | 0.040 | X | 44235439 | missense variant | G/A;T | snv | 0.11 | 1 | ||
| rs371151471 | 1.000 | 0.040 | 6 | 52465092 | missense variant | C/T | snv | 1.2E-03 | 2.0E-04 | 1 | |
| rs3743123 | 1.000 | 0.040 | 15 | 34752856 | synonymous variant | G/A | snv | 0.32 | 0.31 | 1 | |
| rs3752158 | 1.000 | 0.040 | 19 | 607984 | synonymous variant | G/A;C | snv | 1.5E-03; 9.3E-02 | 1 | ||
| rs377286138 | 1.000 | 0.040 | 6 | 52479064 | missense variant | C/T | snv | 1.1E-04 | 7.0E-05 | 1 | |
| rs3804505 | 1.000 | 0.040 | 6 | 52438563 | missense variant | G/A;T | snv | 6.0E-02 | 1 |