rs1736454
From SNPedia
| Merged into | rs707687 |
| Orientation | plus |
| Make rs1736454(C;C) |
| Make rs1736454(C;T) |
| Make rs1736454(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | Y |
| Position | 56978021 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1736454 |
| dbSNP (classic) | rs1736454 |
| ClinGen | rs1736454 |
| ebi | rs1736454 |
| HLI | rs1736454 |
| Exac | rs1736454 |
| Gnomad | rs1736454 |
| Varsome | rs1736454 |
| LitVar | rs1736454 |
| Map | rs1736454 |
| PheGenI | rs1736454 |
| Biobank | rs1736454 |
| 1000 genomes | rs1736454 |
| hgdp | rs1736454 |
| ensembl | rs1736454 |
| geneview | rs1736454 |
| scholar | rs1736454 |
| rs1736454 | |
| pharmgkb | rs1736454 |
| gwascentral | rs1736454 |
| openSNP | rs1736454 |
| 23andMe | rs1736454 |
| SNPshot | rs1736454 |
| SNPdbe | rs1736454 |
| MSV3d | rs1736454 |
| GWAS Ctlg | rs1736454 |
| Y Chrom | rs1736454 |
| Status | Merged into rs707687 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
