rs138273386
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs138273386(A;A) |
| Make rs138273386(A;G) |
| Make rs138273386(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 11 |
| Position | 26994813 |
| Gene | FIBIN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs138273386 |
| dbSNP (classic) | rs138273386 |
| ClinGen | rs138273386 |
| ebi | rs138273386 |
| HLI | rs138273386 |
| Exac | rs138273386 |
| Gnomad | rs138273386 |
| Varsome | rs138273386 |
| LitVar | rs138273386 |
| Map | rs138273386 |
| PheGenI | rs138273386 |
| Biobank | rs138273386 |
| 1000 genomes | rs138273386 |
| hgdp | rs138273386 |
| ensembl | rs138273386 |
| geneview | rs138273386 |
| scholar | rs138273386 |
| rs138273386 | |
| pharmgkb | rs138273386 |
| gwascentral | rs138273386 |
| openSNP | rs138273386 |
| 23andMe | rs138273386 |
| SNPshot | rs138273386 |
| SNPdbe | rs138273386 |
| MSV3d | rs138273386 |
| GWAS Ctlg | rs138273386 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
