rs17170356
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17170356(A;A) |
| Make rs17170356(A;G) |
| Make rs17170356(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 147190776 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17170356 |
| dbSNP (classic) | rs17170356 |
| ClinGen | rs17170356 |
| ebi | rs17170356 |
| HLI | rs17170356 |
| Exac | rs17170356 |
| Gnomad | rs17170356 |
| Varsome | rs17170356 |
| LitVar | rs17170356 |
| Map | rs17170356 |
| PheGenI | rs17170356 |
| Biobank | rs17170356 |
| 1000 genomes | rs17170356 |
| hgdp | rs17170356 |
| ensembl | rs17170356 |
| geneview | rs17170356 |
| scholar | rs17170356 |
| rs17170356 | |
| pharmgkb | rs17170356 |
| gwascentral | rs17170356 |
| openSNP | rs17170356 |
| 23andMe | rs17170356 |
| SNPshot | rs17170356 |
| SNPdbe | rs17170356 |
| MSV3d | rs17170356 |
| GWAS Ctlg | rs17170356 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| 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 | 4E-6 |
| Odds Ratio | .15 [NR] unit increase |
