rs8052655
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8052655(A;A) |
| Make rs8052655(A;G) |
| Make rs8052655(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 16 |
| Position | 67375277 |
| Gene | LRRC36 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8052655 |
| dbSNP (classic) | rs8052655 |
| ClinGen | rs8052655 |
| ebi | rs8052655 |
| HLI | rs8052655 |
| Exac | rs8052655 |
| Gnomad | rs8052655 |
| Varsome | rs8052655 |
| LitVar | rs8052655 |
| Map | rs8052655 |
| PheGenI | rs8052655 |
| Biobank | rs8052655 |
| 1000 genomes | rs8052655 |
| hgdp | rs8052655 |
| ensembl | rs8052655 |
| geneview | rs8052655 |
| scholar | rs8052655 |
| rs8052655 | |
| pharmgkb | rs8052655 |
| gwascentral | rs8052655 |
| openSNP | rs8052655 |
| 23andMe | rs8052655 |
| SNPshot | rs8052655 |
| SNPdbe | rs8052655 |
| MSV3d | rs8052655 |
| GWAS Ctlg | rs8052655 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
