rs5030878
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs5030878(C;C) |
| Make rs5030878(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 51746963 |
| Gene | FPR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5030878 |
| dbSNP (classic) | rs5030878 |
| ClinGen | rs5030878 |
| ebi | rs5030878 |
| HLI | rs5030878 |
| Exac | rs5030878 |
| Gnomad | rs5030878 |
| Varsome | rs5030878 |
| LitVar | rs5030878 |
| Map | rs5030878 |
| PheGenI | rs5030878 |
| Biobank | rs5030878 |
| 1000 genomes | rs5030878 |
| hgdp | rs5030878 |
| ensembl | rs5030878 |
| geneview | rs5030878 |
| scholar | rs5030878 |
| rs5030878 | |
| pharmgkb | rs5030878 |
| gwascentral | rs5030878 |
| openSNP | rs5030878 |
| 23andMe | rs5030878 |
| SNPshot | rs5030878 |
| SNPdbe | rs5030878 |
| MSV3d | rs5030878 |
| GWAS Ctlg | rs5030878 |
| GMAF | 0.1736 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21144844] Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels.
[PMID 23373827
] V101L of human formyl peptide receptor 1 (FPR1) increases receptor affinity and augments the antagonism mediated by cyclosporins.
| ClinVar | |
|---|---|
| Risk | rs5030878(C;C) |
| Alt | rs5030878(C;C) |
| Reference | Rs5030878(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | FPR1 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000019.9:g.52250216A>G |
| CLNSRC | |
| CLNACC | RCV000455423.1, |
