rs9999118
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common genotype |
| Make rs9999118(A;G) |
| Make rs9999118(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 123130312 |
| Gene | SPATA5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9999118 |
| dbSNP (classic) | rs9999118 |
| ClinGen | rs9999118 |
| ebi | rs9999118 |
| HLI | rs9999118 |
| Exac | rs9999118 |
| Gnomad | rs9999118 |
| Varsome | rs9999118 |
| LitVar | rs9999118 |
| Map | rs9999118 |
| PheGenI | rs9999118 |
| Biobank | rs9999118 |
| 1000 genomes | rs9999118 |
| hgdp | rs9999118 |
| ensembl | rs9999118 |
| geneview | rs9999118 |
| scholar | rs9999118 |
| rs9999118 | |
| pharmgkb | rs9999118 |
| gwascentral | rs9999118 |
| openSNP | rs9999118 |
| 23andMe | rs9999118 |
| SNPshot | rs9999118 |
| SNPdbe | rs9999118 |
| MSV3d | rs9999118 |
| GWAS Ctlg | rs9999118 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24797007] |
| Trait | Irritable bowel syndrome |
| Title | Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome. |
| Risk Allele | G |
| P-val | 8E-8 |
| Odds Ratio | 7.30 [3.53-15.03] |
