rs2505535
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2505535(C;C) |
| Make rs2505535(C;T) |
| Make rs2505535(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 43097595 |
| Gene | RET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2505535 |
| dbSNP (classic) | rs2505535 |
| ClinGen | rs2505535 |
| ebi | rs2505535 |
| HLI | rs2505535 |
| Exac | rs2505535 |
| Gnomad | rs2505535 |
| Varsome | rs2505535 |
| LitVar | rs2505535 |
| Map | rs2505535 |
| PheGenI | rs2505535 |
| Biobank | rs2505535 |
| 1000 genomes | rs2505535 |
| hgdp | rs2505535 |
| ensembl | rs2505535 |
| geneview | rs2505535 |
| scholar | rs2505535 |
| rs2505535 | |
| pharmgkb | rs2505535 |
| gwascentral | rs2505535 |
| openSNP | rs2505535 |
| 23andMe | rs2505535 |
| SNPshot | rs2505535 |
| SNPdbe | rs2505535 |
| MSV3d | rs2505535 |
| GWAS Ctlg | rs2505535 |
| GMAF | 0.2576 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18612588] the C allele of rs2505535 would appear to represent a protecting allele for the Chinese population
[PMID 15759212
] Identifying candidate Hirschsprung disease-associated RET variants.
[PMID 20532249] Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.
