rs62623707
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs62623707(A;A) |
| Make rs62623707(A;G) |
| Make rs62623707(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 5 |
| Position | 135952943 |
| Gene | LECT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs62623707 |
| dbSNP (classic) | rs62623707 |
| ClinGen | rs62623707 |
| ebi | rs62623707 |
| HLI | rs62623707 |
| Exac | rs62623707 |
| Gnomad | rs62623707 |
| Varsome | rs62623707 |
| LitVar | rs62623707 |
| Map | rs62623707 |
| PheGenI | rs62623707 |
| Biobank | rs62623707 |
| 1000 genomes | rs62623707 |
| hgdp | rs62623707 |
| ensembl | rs62623707 |
| geneview | rs62623707 |
| scholar | rs62623707 |
| rs62623707 | |
| pharmgkb | rs62623707 |
| gwascentral | rs62623707 |
| openSNP | rs62623707 |
| 23andMe | rs62623707 |
| SNPshot | rs62623707 |
| SNPdbe | rs62623707 |
| MSV3d | rs62623707 |
| GWAS Ctlg | rs62623707 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
