rs776488
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs776488(A;A) |
| Make rs776488(A;C) |
| Make rs776488(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 165034223 |
| Gene | LOC101929658 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs776488 |
| dbSNP (classic) | rs776488 |
| ClinGen | rs776488 |
| ebi | rs776488 |
| HLI | rs776488 |
| Exac | rs776488 |
| Gnomad | rs776488 |
| Varsome | rs776488 |
| LitVar | rs776488 |
| Map | rs776488 |
| PheGenI | rs776488 |
| Biobank | rs776488 |
| 1000 genomes | rs776488 |
| hgdp | rs776488 |
| ensembl | rs776488 |
| geneview | rs776488 |
| scholar | rs776488 |
| rs776488 | |
| pharmgkb | rs776488 |
| gwascentral | rs776488 |
| openSNP | rs776488 |
| 23andMe | rs776488 |
| SNPshot | rs776488 |
| SNPdbe | rs776488 |
| MSV3d | rs776488 |
| GWAS Ctlg | rs776488 |
| GMAF | 0.1694 |
| Max Magnitude | 0 |
[PMID 20585627
] common trait being footedness
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585627]
|
| Trait | Common traits (Other) |
| Title | Web-based, participant-driven studies yield novel genetic associations for common traits |
| Risk Allele | |
| P-val | 2E-7 |
| Odds Ratio | None None |
