rs3764897
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3764897(C;C) |
| Make rs3764897(C;T) |
| Make rs3764897(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 4819581 |
| Gene | PLD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3764897 |
| dbSNP (classic) | rs3764897 |
| ClinGen | rs3764897 |
| ebi | rs3764897 |
| HLI | rs3764897 |
| Exac | rs3764897 |
| Gnomad | rs3764897 |
| Varsome | rs3764897 |
| LitVar | rs3764897 |
| Map | rs3764897 |
| PheGenI | rs3764897 |
| Biobank | rs3764897 |
| 1000 genomes | rs3764897 |
| hgdp | rs3764897 |
| ensembl | rs3764897 |
| geneview | rs3764897 |
| scholar | rs3764897 |
| rs3764897 | |
| pharmgkb | rs3764897 |
| gwascentral | rs3764897 |
| openSNP | rs3764897 |
| 23andMe | rs3764897 |
| SNPshot | rs3764897 |
| SNPdbe | rs3764897 |
| MSV3d | rs3764897 |
| GWAS Ctlg | rs3764897 |
| GMAF | 0.1763 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21308979] Polymorphisms in CHDH gene and the risk of tooth agenesis
[PMID 20011102
] Fine-scale variation and genetic determinants of alternative splicing across individuals.
