rs3893464
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3893464(C;C) |
| Make rs3893464(C;T) |
| Make rs3893464(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 29967473 |
| Gene | HCG2P6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3893464 |
| dbSNP (classic) | rs3893464 |
| ClinGen | rs3893464 |
| ebi | rs3893464 |
| HLI | rs3893464 |
| Exac | rs3893464 |
| Gnomad | rs3893464 |
| Varsome | rs3893464 |
| LitVar | rs3893464 |
| Map | rs3893464 |
| PheGenI | rs3893464 |
| Biobank | rs3893464 |
| 1000 genomes | rs3893464 |
| hgdp | rs3893464 |
| ensembl | rs3893464 |
| geneview | rs3893464 |
| scholar | rs3893464 |
| rs3893464 | |
| pharmgkb | rs3893464 |
| gwascentral | rs3893464 |
| openSNP | rs3893464 |
| 23andMe | rs3893464 |
| SNPshot | rs3893464 |
| SNPdbe | rs3893464 |
| MSV3d | rs3893464 |
| GWAS Ctlg | rs3893464 |
| GMAF | 0.4761 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21900946] |
| Trait | |
| Title | Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. |
| Risk Allele | G |
| P-val | 2E-20 |
| Odds Ratio | 1.5300 [1.39-1.67] |
