rs3006564
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3006564(C;C) |
| Make rs3006564(C;T) |
| Make rs3006564(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 29888959 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3006564 |
| dbSNP (classic) | rs3006564 |
| ClinGen | rs3006564 |
| ebi | rs3006564 |
| HLI | rs3006564 |
| Exac | rs3006564 |
| Gnomad | rs3006564 |
| Varsome | rs3006564 |
| LitVar | rs3006564 |
| Map | rs3006564 |
| PheGenI | rs3006564 |
| Biobank | rs3006564 |
| 1000 genomes | rs3006564 |
| hgdp | rs3006564 |
| ensembl | rs3006564 |
| geneview | rs3006564 |
| scholar | rs3006564 |
| rs3006564 | |
| pharmgkb | rs3006564 |
| gwascentral | rs3006564 |
| openSNP | rs3006564 |
| 23andMe | rs3006564 |
| SNPshot | rs3006564 |
| SNPdbe | rs3006564 |
| MSV3d | rs3006564 |
| GWAS Ctlg | rs3006564 |
| GMAF | 0.4376 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22419666 ]
|
| Trait | |
| Title | Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | 1.3200 None |
