RET
From SNPedia
| is a | gene |
| is | mentioned by |
| EntrezGene | 5979 |
| PheGenI | 5979 |
| VariationViewer | 5979 |
| ClinVar | RET |
| GeneCards | RET |
| dbSNP | 5979 |
| Diseases | RET |
| SADR | 5979 |
| HugeNav | 5979 |
| wikipedia | RET |
| RET | |
| gopubmed | RET |
| EVS | RET |
| HEFalMp | RET |
| MyGene2 | RET |
| 23andMe | RET |
| # SNPs | 107 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs1060500759 | 0 | 43,120,162 | |
| rs121913308 | 0 | 43,114,492 | |
| rs121913309 | 0 | 43,120,165 | |
| rs121913312 | 0 | 43,114,494 | |
| rs121913313 | 0 | 43,113,630 | |
| rs142318626 | 0 | 43,119,587 | |
| rs143795581 | 0 | 43,114,596 | |
| rs143862573 | 0 | 43,119,750 | |
| rs146646971 | 5.1 | 43,114,598 | |
| rs17158558 | 0 | 43,124,887 | |
| rs17857727 | 0 | 43,100,520 | |
| rs1799939 | 0 | 43,114,671 | |
| rs1800858 | 0 | 43,100,520 | |
| rs1800860 | 1 | 43,111,239 | |
| rs1800861 | 0 | 43,118,395 | |
| rs1800862 | 0 | 43,119,646 | |
| rs1800863 | 0 | 43,120,185 | |
| rs1864410 | 0 | 43,080,177 | |
| rs193922699 | 5.1 | 43,114,478 | |
| rs193922700 | 0 | 43,114,680 | |
| rs201740483 | 0 | 43,126,647 | |
| rs2075912 | 0 | 43,126,769 | |
| rs2435357 | 1 | 43,086,608 | |
| rs2472737 | 0 | 43,120,057 | |
| rs2505535 | 0 | 43,097,595 | |
| rs2506004 | 0 | 43,086,825 | |
| rs2506030 | 0 | 42,952,399 | rs2506030 in RET is associated with higher risk in Hirschsprung disease (HSCR) |
| rs2565200 | 0 | 43,127,485 | |
| rs2565206 | 0 | 43,100,333 | |
| rs267607010 | 0 | 43,114,497 | |
| rs267607011 | 0 | 43,120,184 | |
| rs2742234 | 0 | 43,117,161 | |
| rs3026785 | 0 | 43,130,238 | |
| rs34682185 | 0 | 43,106,382 | |
| rs377767389 | 0 | 43,112,120 | |
| rs377767391 | 5.1 | 43,113,627 | |
| rs377767396 | 0 | 43,113,623 | |
| rs377767397 | 0 | 43,113,628 | |
| rs377767398 | 0 | 43,113,628 | |
| rs377767400 | 5.1 | 43,113,650 | |
| rs377767404 | 5.1 | 43,114,488 | |
| rs377767405 | 0 | 43,114,489 | |
| rs377767406 | 0 | 43,114,491 | |
| rs377767408 | 0 | 43,114,496 | |
| rs377767409 | 0 | 43,114,501 | |
| rs377767416 | 0 | 43,118,430 | |
| rs377767422 | 0 | 43,119,635 | |
| rs377767426 | 0 | 43,119,694 | |
| rs377767428 | 0 | 43,120,120 | |
| rs377767429 | 0 | 43,120,120 | |
| ... further results | |||
The RET gene has primarily been associated with risk for Hirschsprung disease.
SNPs in the RET gene associated with Hirschsprung disease include:
- rs3026785
- rs17158558
- rs17857727, now merged into rs1800858
- rs2435357
[PMID 21655256] Familial medullary thyroid carcinoma
