rs212016
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs212016(C;C) |
| Make rs212016(C;T) |
| Make rs212016(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 59995799 |
| Gene | FHIT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs212016 |
| dbSNP (classic) | rs212016 |
| ClinGen | rs212016 |
| ebi | rs212016 |
| HLI | rs212016 |
| Exac | rs212016 |
| Gnomad | rs212016 |
| Varsome | rs212016 |
| LitVar | rs212016 |
| Map | rs212016 |
| PheGenI | rs212016 |
| Biobank | rs212016 |
| 1000 genomes | rs212016 |
| hgdp | rs212016 |
| ensembl | rs212016 |
| geneview | rs212016 |
| scholar | rs212016 |
| rs212016 | |
| pharmgkb | rs212016 |
| gwascentral | rs212016 |
| openSNP | rs212016 |
| 23andMe | rs212016 |
| SNPshot | rs212016 |
| SNPdbe | rs212016 |
| MSV3d | rs212016 |
| GWAS Ctlg | rs212016 |
| GMAF | 0.3485 |
| 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 | 0.000007 |
| Odds Ratio | 1.5400 None |
