rs10499138
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs10499138(A;T) |
| Make rs10499138(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 128171037 |
| Gene | PTPRK |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10499138 |
| dbSNP (classic) | rs10499138 |
| ClinGen | rs10499138 |
| ebi | rs10499138 |
| HLI | rs10499138 |
| Exac | rs10499138 |
| Gnomad | rs10499138 |
| Varsome | rs10499138 |
| LitVar | rs10499138 |
| Map | rs10499138 |
| PheGenI | rs10499138 |
| Biobank | rs10499138 |
| 1000 genomes | rs10499138 |
| hgdp | rs10499138 |
| ensembl | rs10499138 |
| geneview | rs10499138 |
| scholar | rs10499138 |
| rs10499138 | |
| pharmgkb | rs10499138 |
| gwascentral | rs10499138 |
| openSNP | rs10499138 |
| 23andMe | rs10499138 |
| SNPshot | rs10499138 |
| SNPdbe | rs10499138 |
| MSV3d | rs10499138 |
| GWAS Ctlg | rs10499138 |
| GMAF | 0.03444 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 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 | A |
| P-val | 0.000002 |
| Odds Ratio | None None |
