rs34821177
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs34821177(A;A) |
| Make rs34821177(A;G) |
| Make rs34821177(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 5 |
| Position | 126915120 |
| Gene | MARCH3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34821177 |
| dbSNP (classic) | rs34821177 |
| ClinGen | rs34821177 |
| ebi | rs34821177 |
| HLI | rs34821177 |
| Exac | rs34821177 |
| Gnomad | rs34821177 |
| Varsome | rs34821177 |
| LitVar | rs34821177 |
| Map | rs34821177 |
| PheGenI | rs34821177 |
| Biobank | rs34821177 |
| 1000 genomes | rs34821177 |
| hgdp | rs34821177 |
| ensembl | rs34821177 |
| geneview | rs34821177 |
| scholar | rs34821177 |
| rs34821177 | |
| pharmgkb | rs34821177 |
| gwascentral | rs34821177 |
| openSNP | rs34821177 |
| 23andMe | rs34821177 |
| SNPshot | rs34821177 |
| SNPdbe | rs34821177 |
| MSV3d | rs34821177 |
| GWAS Ctlg | rs34821177 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
