rs2228638
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs2228638(A;A) |
| Make rs2228638(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 33186354 |
| Gene | NRP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2228638 |
| dbSNP (classic) | rs2228638 |
| ClinGen | rs2228638 |
| ebi | rs2228638 |
| HLI | rs2228638 |
| Exac | rs2228638 |
| Gnomad | rs2228638 |
| Varsome | rs2228638 |
| LitVar | rs2228638 |
| Map | rs2228638 |
| PheGenI | rs2228638 |
| Biobank | rs2228638 |
| 1000 genomes | rs2228638 |
| hgdp | rs2228638 |
| ensembl | rs2228638 |
| geneview | rs2228638 |
| scholar | rs2228638 |
| rs2228638 | |
| pharmgkb | rs2228638 |
| gwascentral | rs2228638 |
| openSNP | rs2228638 |
| 23andMe | rs2228638 |
| SNPshot | rs2228638 |
| SNPdbe | rs2228638 |
| MSV3d | rs2228638 |
| GWAS Ctlg | rs2228638 |
| GMAF | 0.09642 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23297363 ]
|
| Trait | Tetralogy of Fallot |
| Title | Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot. |
| Risk Allele | A |
| P-val | 2E-7 |
| Odds Ratio | 1.45 [1.239-1.69] |
[PMID 16385451] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
[PMID 29432830] Functional polymorphisms of the neuropilin 1 gene are associated with the risk of tetralogy of Fallot in a Chinese Han population.
