rs312691
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs312691(C;C) |
| Make rs312691(C;T) |
| Make rs312691(T;T) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 17 |
| Position | 70330197 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs312691 |
| dbSNP (classic) | rs312691 |
| ClinGen | rs312691 |
| ebi | rs312691 |
| HLI | rs312691 |
| Exac | rs312691 |
| Gnomad | rs312691 |
| Varsome | rs312691 |
| LitVar | rs312691 |
| Map | rs312691 |
| PheGenI | rs312691 |
| Biobank | rs312691 |
| 1000 genomes | rs312691 |
| hgdp | rs312691 |
| ensembl | rs312691 |
| geneview | rs312691 |
| scholar | rs312691 |
| rs312691 | |
| pharmgkb | rs312691 |
| gwascentral | rs312691 |
| openSNP | rs312691 |
| 23andMe | rs312691 |
| SNPshot | rs312691 |
| SNPdbe | rs312691 |
| MSV3d | rs312691 |
| GWAS Ctlg | rs312691 |
| GMAF | 0.3205 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22863731] |
| Trait | Thyrotoxic hypokalemic periodic paralysis |
| Title | Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3. |
| Risk Allele | C |
| P-val | 8E-14 |
| Odds Ratio | 3.20 [2.40-4.40] |
