rs1079572
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1079572(C;C) |
| Make rs1079572(C;T) |
| Make rs1079572(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 78153241 |
| Gene | WWOX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1079572 |
| dbSNP (classic) | rs1079572 |
| ClinGen | rs1079572 |
| ebi | rs1079572 |
| HLI | rs1079572 |
| Exac | rs1079572 |
| Gnomad | rs1079572 |
| Varsome | rs1079572 |
| LitVar | rs1079572 |
| Map | rs1079572 |
| PheGenI | rs1079572 |
| Biobank | rs1079572 |
| 1000 genomes | rs1079572 |
| hgdp | rs1079572 |
| ensembl | rs1079572 |
| geneview | rs1079572 |
| scholar | rs1079572 |
| rs1079572 | |
| pharmgkb | rs1079572 |
| gwascentral | rs1079572 |
| openSNP | rs1079572 |
| 23andMe | rs1079572 |
| SNPshot | rs1079572 |
| SNPdbe | rs1079572 |
| MSV3d | rs1079572 |
| GWAS Ctlg | rs1079572 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24929828 |
| Trait | Forced vital capacity |
| Title | Genome-wide association analysis identifies six new loci associated with forced vital capacity. |
| Risk Allele | G |
| P-val | 1E-8 |
| Odds Ratio | 16.26 [10.70-21.82] ml increase |
