rs33966734
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs33966734(G;G) |
| Make rs33966734(G;T) |
| Make rs33966734(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 6 |
| Position | 41936060 |
| Gene | CCND3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs33966734 |
| dbSNP (classic) | rs33966734 |
| ClinGen | rs33966734 |
| ebi | rs33966734 |
| HLI | rs33966734 |
| Exac | rs33966734 |
| Gnomad | rs33966734 |
| Varsome | rs33966734 |
| LitVar | rs33966734 |
| Map | rs33966734 |
| PheGenI | rs33966734 |
| Biobank | rs33966734 |
| 1000 genomes | rs33966734 |
| hgdp | rs33966734 |
| ensembl | rs33966734 |
| geneview | rs33966734 |
| scholar | rs33966734 |
| rs33966734 | |
| pharmgkb | rs33966734 |
| gwascentral | rs33966734 |
| openSNP | rs33966734 |
| 23andMe | rs33966734 |
| SNPshot | rs33966734 |
| SNPdbe | rs33966734 |
| MSV3d | rs33966734 |
| GWAS Ctlg | rs33966734 |
| Max Magnitude | 0 |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
