rs3765212
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3765212(G;G) |
| Make rs3765212(G;T) |
| Make rs3765212(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 123438124 |
| Gene | WDYHV1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3765212 |
| dbSNP (classic) | rs3765212 |
| ClinGen | rs3765212 |
| ebi | rs3765212 |
| HLI | rs3765212 |
| Exac | rs3765212 |
| Gnomad | rs3765212 |
| Varsome | rs3765212 |
| LitVar | rs3765212 |
| Map | rs3765212 |
| PheGenI | rs3765212 |
| Biobank | rs3765212 |
| 1000 genomes | rs3765212 |
| hgdp | rs3765212 |
| ensembl | rs3765212 |
| geneview | rs3765212 |
| scholar | rs3765212 |
| rs3765212 | |
| pharmgkb | rs3765212 |
| gwascentral | rs3765212 |
| openSNP | rs3765212 |
| 23andMe | rs3765212 |
| SNPshot | rs3765212 |
| SNPdbe | rs3765212 |
| MSV3d | rs3765212 |
| GWAS Ctlg | rs3765212 |
| GMAF | 0.3843 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18760390
] Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.
