rs229527
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs229527(G;G) |
| Make rs229527(G;T) |
| Make rs229527(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 37185445 |
| Gene | C1QTNF6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs229527 |
| dbSNP (classic) | rs229527 |
| ClinGen | rs229527 |
| ebi | rs229527 |
| HLI | rs229527 |
| Exac | rs229527 |
| Gnomad | rs229527 |
| Varsome | rs229527 |
| LitVar | rs229527 |
| Map | rs229527 |
| PheGenI | rs229527 |
| Biobank | rs229527 |
| 1000 genomes | rs229527 |
| hgdp | rs229527 |
| ensembl | rs229527 |
| geneview | rs229527 |
| scholar | rs229527 |
| rs229527 | |
| pharmgkb | rs229527 |
| gwascentral | rs229527 |
| openSNP | rs229527 |
| 23andMe | rs229527 |
| SNPshot | rs229527 |
| SNPdbe | rs229527 |
| MSV3d | rs229527 |
| GWAS Ctlg | rs229527 |
| GMAF | 0.4619 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20410501 ]
|
| Trait | Vitiligo |
| Title | Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo |
| Risk Allele | T |
| P-val | 2E-16 |
| Odds Ratio | 1.38 [1.28-1.50] |
[PMID 19474294] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
| GWAS snp | |
|---|---|
| PMID | [PMID 23612905] |
| Trait | Graves' disease |
| Title | Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. |
| Risk Allele | |
| P-val | 5E-20 |
| Odds Ratio | 1.23 [1.19-1.3] |
[PMID 28665696] Association Analysis of Single Nucleotide Polymorphisms in C1QTNF6, RAC2, and an Intergenic Region at 14q32.2 with Graves' Disease in Chinese Han Population.
