rs3859192
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3859192(C;C) |
| Make rs3859192(C;T) |
| Make rs3859192(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 39972395 |
| Gene | GSDMA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3859192 |
| dbSNP (classic) | rs3859192 |
| ClinGen | rs3859192 |
| ebi | rs3859192 |
| HLI | rs3859192 |
| Exac | rs3859192 |
| Gnomad | rs3859192 |
| Varsome | rs3859192 |
| LitVar | rs3859192 |
| Map | rs3859192 |
| PheGenI | rs3859192 |
| Biobank | rs3859192 |
| 1000 genomes | rs3859192 |
| hgdp | rs3859192 |
| ensembl | rs3859192 |
| geneview | rs3859192 |
| scholar | rs3859192 |
| rs3859192 | |
| pharmgkb | rs3859192 |
| gwascentral | rs3859192 |
| openSNP | rs3859192 |
| 23andMe | rs3859192 |
| SNPshot | rs3859192 |
| SNPdbe | rs3859192 |
| MSV3d | rs3859192 |
| GWAS Ctlg | rs3859192 |
| GMAF | 0.4229 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22037903 ]
|
| Trait | |
| Title | Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. |
| Risk Allele | |
| P-val | 2E-12 |
| Odds Ratio | 0.1400 None |
[PMID 18310477] ORMDL3 gene is associated with asthma in three ethnically diverse populations.
[PMID 19426955] Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene.
[PMID 22626592] 17q12-21 variants are associated with asthma and interact with active smoking in an adult population from the United Kingdom.
[PMID 28534526] Impact of genetic polymorphisms determining leukocyte/neutrophil count on chemotherapy toxicity.
