rs1456988
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1456988(G;G) |
| Make rs1456988(G;T) |
| Make rs1456988(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 98021670 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1456988 |
| dbSNP (classic) | rs1456988 |
| ClinGen | rs1456988 |
| ebi | rs1456988 |
| HLI | rs1456988 |
| Exac | rs1456988 |
| Gnomad | rs1456988 |
| Varsome | rs1456988 |
| LitVar | rs1456988 |
| Map | rs1456988 |
| PheGenI | rs1456988 |
| Biobank | rs1456988 |
| 1000 genomes | rs1456988 |
| hgdp | rs1456988 |
| ensembl | rs1456988 |
| geneview | rs1456988 |
| scholar | rs1456988 |
| rs1456988 | |
| pharmgkb | rs1456988 |
| gwascentral | rs1456988 |
| openSNP | rs1456988 |
| 23andMe | rs1456988 |
| SNPshot | rs1456988 |
| SNPdbe | rs1456988 |
| MSV3d | rs1456988 |
| GWAS Ctlg | rs1456988 |
| GMAF | 0.4192 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| 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-9 |
| Odds Ratio | 1.12 [1.09-1.18] |
[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.
