rs4703822
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4703822(A;A) |
| Make rs4703822(A;G) |
| Make rs4703822(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 81115402 |
| Gene | RASGRF2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4703822 |
| dbSNP (classic) | rs4703822 |
| ClinGen | rs4703822 |
| ebi | rs4703822 |
| HLI | rs4703822 |
| Exac | rs4703822 |
| Gnomad | rs4703822 |
| Varsome | rs4703822 |
| LitVar | rs4703822 |
| Map | rs4703822 |
| PheGenI | rs4703822 |
| Biobank | rs4703822 |
| 1000 genomes | rs4703822 |
| hgdp | rs4703822 |
| ensembl | rs4703822 |
| geneview | rs4703822 |
| scholar | rs4703822 |
| rs4703822 | |
| pharmgkb | rs4703822 |
| gwascentral | rs4703822 |
| openSNP | rs4703822 |
| 23andMe | rs4703822 |
| SNPshot | rs4703822 |
| SNPdbe | rs4703822 |
| MSV3d | rs4703822 |
| GWAS Ctlg | rs4703822 |
| GMAF | 0.2635 |
| 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 | 0.000004 |
| Odds Ratio | 1.5900 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
