rs3129763
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3129763(A;A) |
| Make rs3129763(A;G) |
| Make rs3129763(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32623148 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3129763 |
| dbSNP (classic) | rs3129763 |
| ClinGen | rs3129763 |
| ebi | rs3129763 |
| HLI | rs3129763 |
| Exac | rs3129763 |
| Gnomad | rs3129763 |
| Varsome | rs3129763 |
| LitVar | rs3129763 |
| Map | rs3129763 |
| PheGenI | rs3129763 |
| Biobank | rs3129763 |
| 1000 genomes | rs3129763 |
| hgdp | rs3129763 |
| ensembl | rs3129763 |
| geneview | rs3129763 |
| scholar | rs3129763 |
| rs3129763 | |
| pharmgkb | rs3129763 |
| gwascentral | rs3129763 |
| openSNP | rs3129763 |
| 23andMe | rs3129763 |
| SNPshot | rs3129763 |
| SNPdbe | rs3129763 |
| MSV3d | rs3129763 |
| GWAS Ctlg | rs3129763 |
| GMAF | 0.2094 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Source nature
Graves' disease or myasthenia gravis rs3129763(C) + rs4639334(C)
| GWAS snp | |
|---|---|
| PMID | [PMID 21779181 ]
|
| Trait | |
| Title | Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. |
| Risk Allele | |
| P-val | 1E-11 |
| Odds Ratio | 1.6500 [1.42-1.91] |
[PMID 19176549] Genome-wide association analysis by lasso penalized logistic regression.
