rs17079928
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17079928(A;A) |
| Make rs17079928(A;G) |
| Make rs17079928(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 24080089 |
| Gene | SPATA13 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17079928 |
| dbSNP (classic) | rs17079928 |
| ClinGen | rs17079928 |
| ebi | rs17079928 |
| HLI | rs17079928 |
| Exac | rs17079928 |
| Gnomad | rs17079928 |
| Varsome | rs17079928 |
| LitVar | rs17079928 |
| Map | rs17079928 |
| PheGenI | rs17079928 |
| Biobank | rs17079928 |
| 1000 genomes | rs17079928 |
| hgdp | rs17079928 |
| ensembl | rs17079928 |
| geneview | rs17079928 |
| scholar | rs17079928 |
| rs17079928 | |
| pharmgkb | rs17079928 |
| gwascentral | rs17079928 |
| openSNP | rs17079928 |
| 23andMe | rs17079928 |
| SNPshot | rs17079928 |
| SNPdbe | rs17079928 |
| MSV3d | rs17079928 |
| GWAS Ctlg | rs17079928 |
| GMAF | 0.2576 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 0.000006 |
| Odds Ratio | 1.3300 None |
