rs13074914
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs13074914(A;A) |
| Make rs13074914(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 54496558 |
| Gene | CACNA2D3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13074914 |
| dbSNP (classic) | rs13074914 |
| ClinGen | rs13074914 |
| ebi | rs13074914 |
| HLI | rs13074914 |
| Exac | rs13074914 |
| Gnomad | rs13074914 |
| Varsome | rs13074914 |
| LitVar | rs13074914 |
| Map | rs13074914 |
| PheGenI | rs13074914 |
| Biobank | rs13074914 |
| 1000 genomes | rs13074914 |
| hgdp | rs13074914 |
| ensembl | rs13074914 |
| geneview | rs13074914 |
| scholar | rs13074914 |
| rs13074914 | |
| pharmgkb | rs13074914 |
| gwascentral | rs13074914 |
| openSNP | rs13074914 |
| 23andMe | rs13074914 |
| SNPshot | rs13074914 |
| SNPdbe | rs13074914 |
| MSV3d | rs13074914 |
| GWAS Ctlg | rs13074914 |
| GMAF | 0.2071 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19061984
] PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.
