rs2565206
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2565206(A;A) |
| Make rs2565206(A;C) |
| Make rs2565206(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 43100333 |
| Gene | RET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2565206 |
| dbSNP (classic) | rs2565206 |
| ClinGen | rs2565206 |
| ebi | rs2565206 |
| HLI | rs2565206 |
| Exac | rs2565206 |
| Gnomad | rs2565206 |
| Varsome | rs2565206 |
| LitVar | rs2565206 |
| Map | rs2565206 |
| PheGenI | rs2565206 |
| Biobank | rs2565206 |
| 1000 genomes | rs2565206 |
| hgdp | rs2565206 |
| ensembl | rs2565206 |
| geneview | rs2565206 |
| scholar | rs2565206 |
| rs2565206 | |
| pharmgkb | rs2565206 |
| gwascentral | rs2565206 |
| openSNP | rs2565206 |
| 23andMe | rs2565206 |
| SNPshot | rs2565206 |
| SNPdbe | rs2565206 |
| MSV3d | rs2565206 |
| GWAS Ctlg | rs2565206 |
| GMAF | 0.3379 |
| Max Magnitude | 0 |
[PMID 23059849] Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form
