| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
| rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 | |
| rs768623239 | 0.662 | 0.640 | 1 | 109689278 | missense variant | A/G | snv | 1.5E-05 | 26 | ||
| rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
| rs1805054 | 0.708 | 0.200 | 1 | 19666020 | synonymous variant | C/T | snv | 0.15; 8.0E-06 | 0.16 | 17 | |
| rs821616 | 0.752 | 0.200 | 1 | 232008852 | missense variant | A/T | snv | 0.26 | 0.29 | 13 | |
| rs2274567 | 0.776 | 0.400 | 1 | 207580276 | missense variant | A/G | snv | 0.25 | 0.21 | 10 | |
| rs6656401 | 0.776 | 0.200 | 1 | 207518704 | intron variant | A/G;T | snv | 8 | |||
| rs6675281 | 0.827 | 0.080 | 1 | 231818355 | missense variant | C/T | snv | 0.11 | 0.14 | 7 | |
| rs3818361 | 0.851 | 0.080 | 1 | 207611623 | intron variant | A/G | snv | 0.74 | 6 | ||
| rs3738401 | 0.882 | 0.080 | 1 | 231694549 | missense variant | G/A | snv | 0.30 | 0.26 | 4 | |
| rs890293 | 0.851 | 0.200 | 1 | 59926822 | upstream gene variant | C/A | snv | 8.6E-02 | 4 | ||
| rs1155002 | 1.000 | 0.080 | 1 | 59908103 | intron variant | T/C | snv | 0.66 | 2 | ||
| rs600491 | 0.925 | 0.080 | 1 | 54867852 | intron variant | C/A;T | snv | 2 | |||
| rs6691117 | 1.000 | 0.080 | 1 | 207609586 | missense variant | A/G | snv | 0.32 | 0.41 | 2 | |
| rs116806486 | 1.000 | 0.080 | 1 | 207523640 | missense variant | A/G | snv | 1.6E-03 | 5.4E-03 | 1 | |
| rs3737002 | 1.000 | 0.080 | 1 | 207587428 | missense variant | C/T | snv | 0.28 | 0.23 | 1 | |
| rs63750207 | 1.000 | 0.080 | 1 | 226891773 | missense variant | C/G;T | snv | 4.4E-05; 4.0E-06 | 1 | ||
| rs1550117 | 0.790 | 0.320 | 2 | 25343038 | upstream gene variant | A/G;T | snv | 11 | |||
| rs744373 | 0.851 | 0.160 | 2 | 127137039 | downstream gene variant | A/G | snv | 0.35 | 8 | ||
| rs13306190 | 0.807 | 0.320 | 2 | 21032408 | missense variant | G/A;C;T | snv | 1.7E-04; 8.0E-06 | 7 | ||
| rs7561528 | 0.882 | 0.080 | 2 | 127132061 | intergenic variant | G/A | snv | 0.28 | 3 |