rs7770227
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7770227(A;A) |
| Make rs7770227(A;G) |
| Make rs7770227(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 114301050 |
| Gene | HS3ST5, LOC101927768 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7770227 |
| dbSNP (classic) | rs7770227 |
| ClinGen | rs7770227 |
| ebi | rs7770227 |
| HLI | rs7770227 |
| Exac | rs7770227 |
| Gnomad | rs7770227 |
| Varsome | rs7770227 |
| LitVar | rs7770227 |
| Map | rs7770227 |
| PheGenI | rs7770227 |
| Biobank | rs7770227 |
| 1000 genomes | rs7770227 |
| hgdp | rs7770227 |
| ensembl | rs7770227 |
| geneview | rs7770227 |
| scholar | rs7770227 |
| rs7770227 | |
| pharmgkb | rs7770227 |
| gwascentral | rs7770227 |
| openSNP | rs7770227 |
| 23andMe | rs7770227 |
| SNPshot | rs7770227 |
| SNPdbe | rs7770227 |
| MSV3d | rs7770227 |
| GWAS Ctlg | rs7770227 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24939585 ]
|
| Trait | Age-related hearing impairment (interaction) |
| Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
| Risk Allele | |
| P-val | 5E-9 |
| Odds Ratio | NR NR |
