rs423955
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs423955(A;A) |
| Make rs423955(A;G) |
| Make rs423955(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 4792339 |
| Gene | RCL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs423955 |
| dbSNP (classic) | rs423955 |
| ClinGen | rs423955 |
| ebi | rs423955 |
| HLI | rs423955 |
| Exac | rs423955 |
| Gnomad | rs423955 |
| Varsome | rs423955 |
| LitVar | rs423955 |
| Map | rs423955 |
| PheGenI | rs423955 |
| Biobank | rs423955 |
| 1000 genomes | rs423955 |
| hgdp | rs423955 |
| ensembl | rs423955 |
| geneview | rs423955 |
| scholar | rs423955 |
| rs423955 | |
| pharmgkb | rs423955 |
| gwascentral | rs423955 |
| openSNP | rs423955 |
| 23andMe | rs423955 |
| SNPshot | rs423955 |
| SNPdbe | rs423955 |
| MSV3d | rs423955 |
| GWAS Ctlg | rs423955 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24026423 ]
|
| Trait | Platelet counts |
| Title | A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. |
| Risk Allele | A |
| P-val | 1E-9 |
| Odds Ratio | 4.94 [NR] unit increase |
