rs6832151
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6832151(G;G) |
| Make rs6832151(G;T) |
| Make rs6832151(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 40301616 |
| Gene | LOC101930098 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6832151 |
| dbSNP (classic) | rs6832151 |
| ClinGen | rs6832151 |
| ebi | rs6832151 |
| HLI | rs6832151 |
| Exac | rs6832151 |
| Gnomad | rs6832151 |
| Varsome | rs6832151 |
| LitVar | rs6832151 |
| Map | rs6832151 |
| PheGenI | rs6832151 |
| Biobank | rs6832151 |
| 1000 genomes | rs6832151 |
| hgdp | rs6832151 |
| ensembl | rs6832151 |
| geneview | rs6832151 |
| scholar | rs6832151 |
| rs6832151 | |
| pharmgkb | rs6832151 |
| gwascentral | rs6832151 |
| openSNP | rs6832151 |
| 23andMe | rs6832151 |
| SNPshot | rs6832151 |
| SNPdbe | rs6832151 |
| MSV3d | rs6832151 |
| GWAS Ctlg | rs6832151 |
| GMAF | 0.2961 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21841780] |
| Trait | |
| Title | A genome-wide association study identifies two new risk loci for Graves' disease. |
| Risk Allele | G |
| P-val | 1E-13 |
| Odds Ratio | 1.2400 [1.17-1.31] |
[PMID 22489947] The replication of the association of the rs6832151 within chromosomal band 4p14 with Graves' disease in a Polish Caucasian population.
[PMID 28521825
] Association of 4p14 and 6q27 variation with Graves disease: a case-control study and a meta-analysis of available evidence.
[PMID 33009792] [Noncoding Polymorphism rs6832151 Is an Attractive Candidate for Genome Editing Aimed at Finding New Molecular Mechanisms of Autoimmune Diseases].
