| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2904880 | 1.000 | 0.040 | 16 | 28933075 | missense variant | C/G | snv | 0.72 | 0.76 | 5 | |
| rs9920 | 1.000 | 0.040 | 7 | 116560038 | 3 prime UTR variant | T/C | snv | 6.7E-02 | 3 | ||
| rs17340351 | 0.925 | 0.040 | 7 | 129068743 | upstream gene variant | T/A | snv | 9.6E-02 | 2 | ||
| rs17612648 | 1.000 | 0.040 | 1 | 198696788 | synonymous variant | C/G;T | snv | 8.8E-03; 8.0E-05 | 2 | ||
| rs4554699 | 0.925 | 0.040 | 1 | 161638578 | intergenic variant | A/G | snv | 2 | |||
| rs7574685 | 0.925 | 0.040 | 2 | 234702877 | intron variant | T/C | snv | 0.59 | 2 | ||
| rs7934606 | 1.000 | 0.040 | 11 | 1100037 | intron variant | C/G;T | snv | 2 | |||
| rs1005714 | 1.000 | 0.040 | 17 | 75228544 | 5 prime UTR variant | G/C | snv | 0.78 | 1 | ||
| rs10186029 | 1.000 | 0.040 | 2 | 213064562 | intron variant | C/T | snv | 0.40 | 1 | ||
| rs10220668 | 1.000 | 0.040 | 14 | 59042487 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs1035798 | 1.000 | 0.040 | 6 | 32183445 | splice region variant | G/A | snv | 0.24 | 0.19 | 1 | |
| rs10406069 | 1.000 | 0.040 | 19 | 35345627 | missense variant | G/A;C | snv | 0.16 | 1 | ||
| rs10413500 | 1.000 | 0.040 | 19 | 35345923 | intron variant | C/G | snv | 0.16 | 1 | ||
| rs10419538 | 1.000 | 0.040 | 19 | 35333116 | intron variant | C/G | snv | 0.11 | 1 | ||
| rs10946216 | 1.000 | 0.040 | 6 | 167125409 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs11102522 | 1.000 | 0.040 | 1 | 112708266 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs11117420 | 1.000 | 0.040 | 16 | 85938316 | intron variant | G/C;T | snv | 1 | |||
| rs11171747 | 1.000 | 0.040 | 12 | 56124624 | 3 prime UTR variant | T/A;G | snv | 1 | |||
| rs11217020 | 1.000 | 0.040 | 11 | 118768644 | intron variant | G/A;C | snv | 1 | |||
| rs11538960 | 1.000 | 0.040 | 1 | 112701565 | missense variant | C/T | snv | 4.2E-04 | 5.2E-04 | 1 | |
| rs12039904 | 1.000 | 0.040 | 1 | 173243134 | intergenic variant | C/T | snv | 0.19 | 1 | ||
| rs12534421 | 1.000 | 0.040 | 7 | 128984019 | intron variant | C/A | snv | 9.0E-02 | 1 | ||
| rs1328142 | 1.000 | 0.040 | 9 | 70783498 | intron variant | C/A | snv | 0.21 | 1 | ||
| rs16832798 | 1.000 | 0.040 | 2 | 190669646 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs17424921 | 1.000 | 0.040 | 7 | 129068068 | upstream gene variant | G/C | snv | 0.11 | 1 |