rs1450100
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1450100(A;A) |
| Make rs1450100(A;C) |
| Make rs1450100(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 7496515 |
| Gene | GRM7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1450100 |
| dbSNP (classic) | rs1450100 |
| ClinGen | rs1450100 |
| ebi | rs1450100 |
| HLI | rs1450100 |
| Exac | rs1450100 |
| Gnomad | rs1450100 |
| Varsome | rs1450100 |
| LitVar | rs1450100 |
| Map | rs1450100 |
| PheGenI | rs1450100 |
| Biobank | rs1450100 |
| 1000 genomes | rs1450100 |
| hgdp | rs1450100 |
| ensembl | rs1450100 |
| geneview | rs1450100 |
| scholar | rs1450100 |
| rs1450100 | |
| pharmgkb | rs1450100 |
| gwascentral | rs1450100 |
| openSNP | rs1450100 |
| 23andMe | rs1450100 |
| SNPshot | rs1450100 |
| SNPdbe | rs1450100 |
| MSV3d | rs1450100 |
| GWAS Ctlg | rs1450100 |
| GMAF | 0.3393 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 0.000008 |
| Odds Ratio | 1.5400 None |
