| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs77724903 | 0.672 | 0.280 | 10 | 43118460 | missense variant | A/G;T | snv | 4.0E-06; 2.1E-03 | 4 | ||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
| rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 2 | |||
| rs2904551 | 0.776 | 0.160 | 22 | 18918421 | missense variant | A/G | snv | 5.2E-03 | 2.8E-03 | 2 | |
| rs1402272180 | 1.000 | 0.040 | 1 | 243637661 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs373191257 | 0.827 | 0.080 | 16 | 56363027 | missense variant | T/A | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs76151636 | 0.776 | 0.280 | 13 | 51944145 | missense variant | G/A;T | snv | 4.0E-06; 9.2E-04 | 1 | ||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
| rs770462360 | 1.000 | 0.040 | 11 | 64839070 | missense variant | G/A | snv | 2.0E-05 | 1 | ||
| rs1384093596 | 1.000 | 0.040 | 12 | 67657500 | missense variant | C/T | snv | 1 | |||
| rs63750949 | 0.827 | 0.080 | 2 | 47806213 | missense variant | C/A;T | snv | 1 | |||
| rs779221554 | 1.000 | 0.040 | X | 109430395 | missense variant | C/A;T | snv | 1 | |||
| rs1057519903 | 0.683 | 0.080 | 1 | 226064434 | missense variant | A/T | snv | 1 | |||
| rs1553260624 | 0.763 | 0.080 | 1 | 226064454 | missense variant | G/A | snv | 1 | |||
| rs1057519904 | 0.742 | 0.080 | 6 | 27872233 | missense variant | T/A | snv | 1 | |||
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs121913503 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 1 | |||
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 1 | |
| rs375412266 | 1.000 | 0.040 | 3 | 50617647 | missense variant | C/G;T | snv | 2.1E-04; 4.1E-06 | 1 | ||
| rs17855787 | 1.000 | 0.040 | 17 | 50109341 | missense variant | G/A | snv | 1 | |||
| rs371854396 | 1.000 | 0.040 | 1 | 20638098 | missense variant | C/G;T | snv | 1.6E-05; 4.0E-06 | 1 | ||
| rs1466858740 | 1.000 | 0.040 | 16 | 24180881 | missense variant | G/A | snv | 1 | |||
| rs121909218 | 0.672 | 0.360 | 10 | 87933145 | missense variant | G/A | snv | 1 | |||
| rs562015640 | 0.742 | 0.360 | 10 | 87960957 | stop gained | A/G;T | snv | 1.2E-05 | 1 |