rs34815962
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs34815962(C;C) |
| Make rs34815962(C;T) |
| Make rs34815962(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 15 |
| Position | 72169914 |
| Gene | GRAMD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34815962 |
| dbSNP (classic) | rs34815962 |
| ClinGen | rs34815962 |
| ebi | rs34815962 |
| HLI | rs34815962 |
| Exac | rs34815962 |
| Gnomad | rs34815962 |
| Varsome | rs34815962 |
| LitVar | rs34815962 |
| Map | rs34815962 |
| PheGenI | rs34815962 |
| Biobank | rs34815962 |
| 1000 genomes | rs34815962 |
| hgdp | rs34815962 |
| ensembl | rs34815962 |
| geneview | rs34815962 |
| scholar | rs34815962 |
| rs34815962 | |
| pharmgkb | rs34815962 |
| gwascentral | rs34815962 |
| openSNP | rs34815962 |
| 23andMe | rs34815962 |
| SNPshot | rs34815962 |
| SNPdbe | rs34815962 |
| MSV3d | rs34815962 |
| GWAS Ctlg | rs34815962 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
