| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908212 | 0.732 | 0.160 | 19 | 13303877 | missense variant | G/A | snv | 14 | |||
| rs121918799 | 0.752 | 0.120 | 2 | 166015636 | missense variant | G/C | snv | 1.7E-03 | 1.6E-03 | 14 | |
| rs121908225 | 0.790 | 0.120 | 19 | 13365448 | missense variant | G/A | snv | 12 | |||
| rs1057520918 | 0.790 | 0.160 | 19 | 13262780 | missense variant | C/T | snv | 11 | |||
| rs121908217 | 0.851 | 0.120 | 19 | 13308452 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
| rs746795369 | 0.827 | 0.080 | 1 | 160139969 | missense variant | C/A;T | snv | 1.2E-05; 4.0E-06 | 6 | ||
| rs121908230 | 0.882 | 0.080 | 19 | 13262789 | missense variant | C/T | snv | 5 | |||
| rs587777771 | 0.851 | 0.240 | 19 | 41970275 | missense variant | C/T | snv | 4 | |||
| rs1345986424 | 0.851 | 0.160 | 1 | 42943291 | stop gained | C/A;T | snv | 4 | |||
| rs782461379 | 0.882 | 0.120 | 19 | 41988511 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 7.0E-06 | 3 | |
| rs1164174661 | 0.925 | 0.120 | 19 | 13283358 | missense variant | T/C | snv | 3 | |||
| rs782503624 | 0.925 | 0.240 | 19 | 41970308 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs763054302 | 1.000 | 0.040 | 19 | 13299007 | missense variant | C/T | snv | 8.5E-05 | 4.9E-05 | 2 | |
| rs1253956567 | 1.000 | 0.040 | 2 | 166038072 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 2 |