rs555895
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs555895(G;G) |
| Make rs555895(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 87961150 |
| Gene | PTEN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs555895 |
| dbSNP (classic) | rs555895 |
| ClinGen | rs555895 |
| ebi | rs555895 |
| HLI | rs555895 |
| Exac | rs555895 |
| Gnomad | rs555895 |
| Varsome | rs555895 |
| LitVar | rs555895 |
| Map | rs555895 |
| PheGenI | rs555895 |
| Biobank | rs555895 |
| 1000 genomes | rs555895 |
| hgdp | rs555895 |
| ensembl | rs555895 |
| geneview | rs555895 |
| scholar | rs555895 |
| rs555895 | |
| pharmgkb | rs555895 |
| gwascentral | rs555895 |
| openSNP | rs555895 |
| 23andMe | rs555895 |
| SNPshot | rs555895 |
| SNPdbe | rs555895 |
| MSV3d | rs555895 |
| GWAS Ctlg | rs555895 |
| GMAF | 0.4339 |
| Max Magnitude | 0 |
[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.
| ClinVar | |
|---|---|
| Risk | rs555895(G;G) |
| Alt | rs555895(G;G) |
| Reference | Rs555895(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | PTEN |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000010.10:g.89720907T>G |
| CLNSRC | ClinVar |
| CLNACC | RCV000078603.4, |
[PMID 26541596] Association of genetic polymorphisms in PTEN and additional gene-gene interaction with risk of esophageal squamous cell carcinoma in Chinese Han population
