rs457717
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs457717(A;A) |
| Make rs457717(A;G) |
| Make rs457717(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 76625147 |
| Gene | F2RL2, IQGAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs457717 |
| dbSNP (classic) | rs457717 |
| ClinGen | rs457717 |
| ebi | rs457717 |
| HLI | rs457717 |
| Exac | rs457717 |
| Gnomad | rs457717 |
| Varsome | rs457717 |
| LitVar | rs457717 |
| Map | rs457717 |
| PheGenI | rs457717 |
| Biobank | rs457717 |
| 1000 genomes | rs457717 |
| hgdp | rs457717 |
| ensembl | rs457717 |
| geneview | rs457717 |
| scholar | rs457717 |
| rs457717 | |
| pharmgkb | rs457717 |
| gwascentral | rs457717 |
| openSNP | rs457717 |
| 23andMe | rs457717 |
| SNPshot | rs457717 |
| SNPdbe | rs457717 |
| MSV3d | rs457717 |
| GWAS Ctlg | rs457717 |
| GMAF | 0.3935 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20068591 ]
|
| Trait | Hearing impairment |
| Title | A genome-wide association study for age-related hearing impairment in the Saami |
| Risk Allele | T |
| P-val | 4E-7 |
| Odds Ratio | None None |
[PMID 26187738] The European GWAS-identified risk SNP rs457717 within IQGAP2 is not associated with age-related hearing impairment in Han male Chinese population
