rs2075575
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2075575(C;C) |
| Make rs2075575(C;T) |
| Make rs2075575(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 26866562 |
| Gene | AQP4, AQP4-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2075575 |
| dbSNP (classic) | rs2075575 |
| ClinGen | rs2075575 |
| ebi | rs2075575 |
| HLI | rs2075575 |
| Exac | rs2075575 |
| Gnomad | rs2075575 |
| Varsome | rs2075575 |
| LitVar | rs2075575 |
| Map | rs2075575 |
| PheGenI | rs2075575 |
| Biobank | rs2075575 |
| 1000 genomes | rs2075575 |
| hgdp | rs2075575 |
| ensembl | rs2075575 |
| geneview | rs2075575 |
| scholar | rs2075575 |
| rs2075575 | |
| pharmgkb | rs2075575 |
| gwascentral | rs2075575 |
| openSNP | rs2075575 |
| 23andMe | rs2075575 |
| SNPshot | rs2075575 |
| SNPdbe | rs2075575 |
| MSV3d | rs2075575 |
| GWAS Ctlg | rs2075575 |
| GMAF | 0.2736 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20351659] Aquaporin-4 gene variation and sudden infant death syndrome
[PMID 23352976] Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor alpha in patients with Meniere's disease and sudden sensorineural hearing loss.
