rs1402366
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1402366(G;G) |
| Make rs1402366(G;T) |
| Make rs1402366(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 22724978 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1402366 |
| dbSNP (classic) | rs1402366 |
| ClinGen | rs1402366 |
| ebi | rs1402366 |
| HLI | rs1402366 |
| Exac | rs1402366 |
| Gnomad | rs1402366 |
| Varsome | rs1402366 |
| LitVar | rs1402366 |
| Map | rs1402366 |
| PheGenI | rs1402366 |
| Biobank | rs1402366 |
| 1000 genomes | rs1402366 |
| hgdp | rs1402366 |
| ensembl | rs1402366 |
| geneview | rs1402366 |
| scholar | rs1402366 |
| rs1402366 | |
| pharmgkb | rs1402366 |
| gwascentral | rs1402366 |
| openSNP | rs1402366 |
| 23andMe | rs1402366 |
| SNPshot | rs1402366 |
| SNPdbe | rs1402366 |
| MSV3d | rs1402366 |
| GWAS Ctlg | rs1402366 |
| GMAF | 0.1042 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19061984
] PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
