rs4900109
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4900109(G;G) |
| Make rs4900109(G;T) |
| Make rs4900109(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 92297047 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4900109 |
| dbSNP (classic) | rs4900109 |
| ClinGen | rs4900109 |
| ebi | rs4900109 |
| HLI | rs4900109 |
| Exac | rs4900109 |
| Gnomad | rs4900109 |
| Varsome | rs4900109 |
| LitVar | rs4900109 |
| Map | rs4900109 |
| PheGenI | rs4900109 |
| Biobank | rs4900109 |
| 1000 genomes | rs4900109 |
| hgdp | rs4900109 |
| ensembl | rs4900109 |
| geneview | rs4900109 |
| scholar | rs4900109 |
| rs4900109 | |
| pharmgkb | rs4900109 |
| gwascentral | rs4900109 |
| openSNP | rs4900109 |
| 23andMe | rs4900109 |
| SNPshot | rs4900109 |
| SNPdbe | rs4900109 |
| MSV3d | rs4900109 |
| GWAS Ctlg | rs4900109 |
| GMAF | 0.2934 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21835309 ]
|
| Trait | |
| Title | GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. |
| Risk Allele | G |
| P-val | 8E-21 |
| Odds Ratio | 0.1700 [0.13-0.21] unit increase |
