rs17880989
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs17880989(A;A) |
| Make rs17880989(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 14 |
| Position | 22844424 |
| Gene | MMP14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17880989 |
| dbSNP (classic) | rs17880989 |
| ClinGen | rs17880989 |
| ebi | rs17880989 |
| HLI | rs17880989 |
| Exac | rs17880989 |
| Gnomad | rs17880989 |
| Varsome | rs17880989 |
| LitVar | rs17880989 |
| Map | rs17880989 |
| PheGenI | rs17880989 |
| Biobank | rs17880989 |
| 1000 genomes | rs17880989 |
| hgdp | rs17880989 |
| ensembl | rs17880989 |
| geneview | rs17880989 |
| scholar | rs17880989 |
| rs17880989 | |
| pharmgkb | rs17880989 |
| gwascentral | rs17880989 |
| openSNP | rs17880989 |
| 23andMe | rs17880989 |
| SNPshot | rs17880989 |
| SNPdbe | rs17880989 |
| MSV3d | rs17880989 |
| GWAS Ctlg | rs17880989 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
