| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587778776 | 1.000 | 0.120 | 4 | 1804396 | missense variant | T/A;G | snv | 1.2E-05 | 1 | ||
| rs17881656 | 0.925 | 0.240 | 4 | 1804404 | missense variant | T/A;C | snv | 8.0E-06; 3.3E-03 | 3 | ||
| rs28931615 | 0.732 | 0.240 | 4 | 1804426 | missense variant | C/A;T | snv | 13 | |||
| rs761896295 | 1.000 | 0.080 | 4 | 1804450 | missense variant | G/A | snv | 2.4E-05 | 2.1E-05 | 2 | |
| rs3135890 | 4 | 1804792 | non coding transcript exon variant | C/A;T | snv | 0.12 | 1 | ||||
| rs56240927 | 1.000 | 0.080 | 4 | 1804906 | missense variant | C/T | snv | 1.3E-03 | 8.2E-04 | 1 | |
| rs533045918 | 1.000 | 0.040 | 4 | 1804968 | missense variant | C/G;T | snv | 2.6E-05 | 1 | ||
| rs267606808 | 0.882 | 0.120 | 4 | 1805396 | missense variant | A/G | snv | 3 | |||
| rs1292564852 | 1.000 | 4 | 1805414 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
| rs121913112 | 1.000 | 0.280 | 4 | 1805561 | missense variant | G/A;C | snv | 4.8E-05; 4.0E-06 | 1 | ||
| rs751213196 | 1.000 | 0.120 | 4 | 1805602 | missense variant | G/A;T | snv | 1.2E-05; 4.0E-06 | 1 | ||
| rs1448843898 | 1.000 | 0.120 | 4 | 1805608 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs80053154 | 0.925 | 0.120 | 4 | 1805636 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs1211533350 | 0.827 | 0.120 | 4 | 1805638 | synonymous variant | C/A | snv | 4.0E-06 | 7.0E-06 | 5 | |
| rs77722678 | 1.000 | 0.120 | 4 | 1805643 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs28933068 | 0.645 | 0.560 | 4 | 1805644 | missense variant | C/A;G;T | snv | 1.6E-05 | 30 | ||
| rs587777857 | 1.000 | 0.200 | 4 | 1805661 | missense variant | C/A;T | snv | 1 | |||
| rs121913113 | 0.882 | 0.240 | 4 | 1806076 | missense variant | G/A | snv | 3 | |||
| rs1453271838 | 1.000 | 0.280 | 4 | 1806096 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
| rs587779383 | 0.851 | 0.120 | 4 | 1806157 | missense variant | A/C;G;T | snv | 5 | |||
| rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 25 | ||
| rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 30 | |||
| rs28928868 | 0.925 | 0.120 | 4 | 1806164 | missense variant | G/C;T | snv | 4.0E-06 | 2 | ||
| rs121913480 | 1.000 | 0.120 | 4 | 1806604 | missense variant | G/T | snv | 2 | |||
| rs1325547001 | 1.000 | 0.040 | 4 | 1806619 | missense variant | G/A | snv | 4.0E-06 | 2 |