rs41274586
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs41274586(A;A) |
| Make rs41274586(A;G) |
| Make rs41274586(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 10 |
| Position | 77821218 |
| Gene | DLG5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41274586 |
| dbSNP (classic) | rs41274586 |
| ClinGen | rs41274586 |
| ebi | rs41274586 |
| HLI | rs41274586 |
| Exac | rs41274586 |
| Gnomad | rs41274586 |
| Varsome | rs41274586 |
| LitVar | rs41274586 |
| Map | rs41274586 |
| PheGenI | rs41274586 |
| Biobank | rs41274586 |
| 1000 genomes | rs41274586 |
| hgdp | rs41274586 |
| ensembl | rs41274586 |
| geneview | rs41274586 |
| scholar | rs41274586 |
| rs41274586 | |
| pharmgkb | rs41274586 |
| gwascentral | rs41274586 |
| openSNP | rs41274586 |
| 23andMe | rs41274586 |
| SNPshot | rs41274586 |
| SNPdbe | rs41274586 |
| MSV3d | rs41274586 |
| GWAS Ctlg | rs41274586 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
