rs2565200
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2565200(A;A) |
| Make rs2565200(A;G) |
| Make rs2565200(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 43127485 |
| Gene | RET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2565200 |
| dbSNP (classic) | rs2565200 |
| ClinGen | rs2565200 |
| ebi | rs2565200 |
| HLI | rs2565200 |
| Exac | rs2565200 |
| Gnomad | rs2565200 |
| Varsome | rs2565200 |
| LitVar | rs2565200 |
| Map | rs2565200 |
| PheGenI | rs2565200 |
| Biobank | rs2565200 |
| 1000 genomes | rs2565200 |
| hgdp | rs2565200 |
| ensembl | rs2565200 |
| geneview | rs2565200 |
| scholar | rs2565200 |
| rs2565200 | |
| pharmgkb | rs2565200 |
| gwascentral | rs2565200 |
| openSNP | rs2565200 |
| 23andMe | rs2565200 |
| SNPshot | rs2565200 |
| SNPdbe | rs2565200 |
| MSV3d | rs2565200 |
| GWAS Ctlg | rs2565200 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24897126
] RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease
[PMID 27798940] Rare RET Variant p.D707E in a Chinese Pedigree with Hereditary Medullary Thyroid Carcinoma.
