rs141308595
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs141308595(G;G) |
| Make rs141308595(G;T) |
| Make rs141308595(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 15 |
| Position | 88881639 |
| Gene | HAPLN3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141308595 |
| dbSNP (classic) | rs141308595 |
| ClinGen | rs141308595 |
| ebi | rs141308595 |
| HLI | rs141308595 |
| Exac | rs141308595 |
| Gnomad | rs141308595 |
| Varsome | rs141308595 |
| LitVar | rs141308595 |
| Map | rs141308595 |
| PheGenI | rs141308595 |
| Biobank | rs141308595 |
| 1000 genomes | rs141308595 |
| hgdp | rs141308595 |
| ensembl | rs141308595 |
| geneview | rs141308595 |
| scholar | rs141308595 |
| rs141308595 | |
| pharmgkb | rs141308595 |
| gwascentral | rs141308595 |
| openSNP | rs141308595 |
| 23andMe | rs141308595 |
| SNPshot | rs141308595 |
| SNPdbe | rs141308595 |
| MSV3d | rs141308595 |
| GWAS Ctlg | rs141308595 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
