rs17431184
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17431184(C;C) |
| Make rs17431184(C;T) |
| Make rs17431184(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 87960494 |
| Gene | PTEN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17431184 |
| dbSNP (classic) | rs17431184 |
| ClinGen | rs17431184 |
| ebi | rs17431184 |
| HLI | rs17431184 |
| Exac | rs17431184 |
| Gnomad | rs17431184 |
| Varsome | rs17431184 |
| LitVar | rs17431184 |
| Map | rs17431184 |
| PheGenI | rs17431184 |
| Biobank | rs17431184 |
| 1000 genomes | rs17431184 |
| hgdp | rs17431184 |
| ensembl | rs17431184 |
| geneview | rs17431184 |
| scholar | rs17431184 |
| rs17431184 | |
| pharmgkb | rs17431184 |
| gwascentral | rs17431184 |
| openSNP | rs17431184 |
| 23andMe | rs17431184 |
| SNPshot | rs17431184 |
| SNPdbe | rs17431184 |
| MSV3d | rs17431184 |
| GWAS Ctlg | rs17431184 |
| GMAF | 0.1478 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23068025] Association of PTEN genetic polymorphisms with atherosclerotic cerebral infarction in the Han Chinese population
[PMID 17033968
] Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.
[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
[PMID 26541596] Association of genetic polymorphisms in PTEN and additional gene-gene interaction with risk of esophageal squamous cell carcinoma in Chinese Han population
