rs61680841
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs61680841(A;A) |
| Make rs61680841(A;T) |
| Make rs61680841(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 15 |
| Position | 91273113 |
| Gene | SV2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61680841 |
| dbSNP (classic) | rs61680841 |
| ClinGen | rs61680841 |
| ebi | rs61680841 |
| HLI | rs61680841 |
| Exac | rs61680841 |
| Gnomad | rs61680841 |
| Varsome | rs61680841 |
| LitVar | rs61680841 |
| Map | rs61680841 |
| PheGenI | rs61680841 |
| Biobank | rs61680841 |
| 1000 genomes | rs61680841 |
| hgdp | rs61680841 |
| ensembl | rs61680841 |
| geneview | rs61680841 |
| scholar | rs61680841 |
| rs61680841 | |
| pharmgkb | rs61680841 |
| gwascentral | rs61680841 |
| openSNP | rs61680841 |
| 23andMe | rs61680841 |
| SNPshot | rs61680841 |
| SNPdbe | rs61680841 |
| MSV3d | rs61680841 |
| GWAS Ctlg | rs61680841 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24939585 ]
|
| Trait | Age-related hearing impairment |
| Title | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
| Risk Allele | |
| P-val | 6E-6 |
| Odds Ratio | .10 [NR] unit decrease |
