rs675482
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs675482(C;C) |
| Make rs675482(C;T) |
| Make rs675482(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 128856699 |
| Gene | KCNJ1, LOC107984409 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs675482 |
| dbSNP (classic) | rs675482 |
| ClinGen | rs675482 |
| ebi | rs675482 |
| HLI | rs675482 |
| Exac | rs675482 |
| Gnomad | rs675482 |
| Varsome | rs675482 |
| LitVar | rs675482 |
| Map | rs675482 |
| PheGenI | rs675482 |
| Biobank | rs675482 |
| 1000 genomes | rs675482 |
| hgdp | rs675482 |
| ensembl | rs675482 |
| geneview | rs675482 |
| scholar | rs675482 |
| rs675482 | |
| pharmgkb | rs675482 |
| gwascentral | rs675482 |
| openSNP | rs675482 |
| 23andMe | rs675482 |
| SNPshot | rs675482 |
| SNPdbe | rs675482 |
| MSV3d | rs675482 |
| GWAS Ctlg | rs675482 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26313793
] Clinical and Genetic Factors Associated With Thiazide-Induced Hyponatremia
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
