rs7040561
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7040561(A;A) |
| Make rs7040561(A;T) |
| Make rs7040561(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 125766699 |
| Gene | PBX3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7040561 |
| dbSNP (classic) | rs7040561 |
| ClinGen | rs7040561 |
| ebi | rs7040561 |
| HLI | rs7040561 |
| Exac | rs7040561 |
| Gnomad | rs7040561 |
| Varsome | rs7040561 |
| LitVar | rs7040561 |
| Map | rs7040561 |
| PheGenI | rs7040561 |
| Biobank | rs7040561 |
| 1000 genomes | rs7040561 |
| hgdp | rs7040561 |
| ensembl | rs7040561 |
| geneview | rs7040561 |
| scholar | rs7040561 |
| rs7040561 | |
| pharmgkb | rs7040561 |
| gwascentral | rs7040561 |
| openSNP | rs7040561 |
| 23andMe | rs7040561 |
| SNPshot | rs7040561 |
| SNPdbe | rs7040561 |
| MSV3d | rs7040561 |
| GWAS Ctlg | rs7040561 |
| GMAF | 0.09688 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19626039] Lack of replication of celiac disease risk variants reported in a Spanish population using an independent Spanish sample
[PMID 18241860] Combined functional and positional gene information for the identification of susceptibility variants in celiac disease.
[PMID 18471539
] No evidence in a large UK collection for celiac disease risk variants reported by a Spanish study.
