rs41292521
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs41292521(A;A) |
| Make rs41292521(A;G) |
| Make rs41292521(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 51408295 |
| Gene | EPS15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41292521 |
| dbSNP (classic) | rs41292521 |
| ClinGen | rs41292521 |
| ebi | rs41292521 |
| HLI | rs41292521 |
| Exac | rs41292521 |
| Gnomad | rs41292521 |
| Varsome | rs41292521 |
| LitVar | rs41292521 |
| Map | rs41292521 |
| PheGenI | rs41292521 |
| Biobank | rs41292521 |
| 1000 genomes | rs41292521 |
| hgdp | rs41292521 |
| ensembl | rs41292521 |
| geneview | rs41292521 |
| scholar | rs41292521 |
| rs41292521 | |
| pharmgkb | rs41292521 |
| gwascentral | rs41292521 |
| openSNP | rs41292521 |
| 23andMe | rs41292521 |
| SNPshot | rs41292521 |
| SNPdbe | rs41292521 |
| MSV3d | rs41292521 |
| GWAS Ctlg | rs41292521 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
