rs1878935
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1878935(A;A) |
| Make rs1878935(A;G) |
| Make rs1878935(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 158535077 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1878935 |
| dbSNP (classic) | rs1878935 |
| ClinGen | rs1878935 |
| ebi | rs1878935 |
| HLI | rs1878935 |
| Exac | rs1878935 |
| Gnomad | rs1878935 |
| Varsome | rs1878935 |
| LitVar | rs1878935 |
| Map | rs1878935 |
| PheGenI | rs1878935 |
| Biobank | rs1878935 |
| 1000 genomes | rs1878935 |
| hgdp | rs1878935 |
| ensembl | rs1878935 |
| geneview | rs1878935 |
| scholar | rs1878935 |
| rs1878935 | |
| pharmgkb | rs1878935 |
| gwascentral | rs1878935 |
| openSNP | rs1878935 |
| 23andMe | rs1878935 |
| SNPshot | rs1878935 |
| SNPdbe | rs1878935 |
| MSV3d | rs1878935 |
| GWAS Ctlg | rs1878935 |
| 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 | 9E-9 |
| Odds Ratio | NR NR |
