rs1329189
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1329189(C;C) |
| Make rs1329189(C;T) |
| Make rs1329189(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 128200108 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1329189 |
| dbSNP (classic) | rs1329189 |
| ClinGen | rs1329189 |
| ebi | rs1329189 |
| HLI | rs1329189 |
| Exac | rs1329189 |
| Gnomad | rs1329189 |
| Varsome | rs1329189 |
| LitVar | rs1329189 |
| Map | rs1329189 |
| PheGenI | rs1329189 |
| Biobank | rs1329189 |
| 1000 genomes | rs1329189 |
| hgdp | rs1329189 |
| ensembl | rs1329189 |
| geneview | rs1329189 |
| scholar | rs1329189 |
| rs1329189 | |
| pharmgkb | rs1329189 |
| gwascentral | rs1329189 |
| openSNP | rs1329189 |
| 23andMe | rs1329189 |
| SNPshot | rs1329189 |
| SNPdbe | rs1329189 |
| MSV3d | rs1329189 |
| GWAS Ctlg | rs1329189 |
| GMAF | 0.3131 |
| 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 | 1.3000 None |
