rs1566667
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | |
| (A;G) | 0 | |
| (G;G) | 0 |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 130127245 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1566667 |
| dbSNP (classic) | rs1566667 |
| ClinGen | rs1566667 |
| ebi | rs1566667 |
| HLI | rs1566667 |
| Exac | rs1566667 |
| Gnomad | rs1566667 |
| Varsome | rs1566667 |
| LitVar | rs1566667 |
| Map | rs1566667 |
| PheGenI | rs1566667 |
| Biobank | rs1566667 |
| 1000 genomes | rs1566667 |
| hgdp | rs1566667 |
| ensembl | rs1566667 |
| geneview | rs1566667 |
| scholar | rs1566667 |
| rs1566667 | |
| pharmgkb | rs1566667 |
| gwascentral | rs1566667 |
| openSNP | rs1566667 |
| 23andMe | rs1566667 |
| SNPshot | rs1566667 |
| SNPdbe | rs1566667 |
| MSV3d | rs1566667 |
| GWAS Ctlg | rs1566667 |
| GMAF | 0.2319 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
This SNP, rs1566667, was mentioned as one of the SNPs defining a haplotype used during a search for a deafness-associated gene on chromosome 12. However, rs1566667 itself has no reported associations with deafness (or any other condition).
[PMID 16195816] Refinement of the DFNA41 locus and candidate genes analysis.
