rs1956529
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1956529(A;A) |
| Make rs1956529(A;G) |
| Make rs1956529(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 68322207 |
| Gene | RAD51B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1956529 |
| dbSNP (classic) | rs1956529 |
| ClinGen | rs1956529 |
| ebi | rs1956529 |
| HLI | rs1956529 |
| Exac | rs1956529 |
| Gnomad | rs1956529 |
| Varsome | rs1956529 |
| LitVar | rs1956529 |
| Map | rs1956529 |
| PheGenI | rs1956529 |
| Biobank | rs1956529 |
| 1000 genomes | rs1956529 |
| hgdp | rs1956529 |
| ensembl | rs1956529 |
| geneview | rs1956529 |
| scholar | rs1956529 |
| rs1956529 | |
| pharmgkb | rs1956529 |
| gwascentral | rs1956529 |
| openSNP | rs1956529 |
| 23andMe | rs1956529 |
| SNPshot | rs1956529 |
| SNPdbe | rs1956529 |
| MSV3d | rs1956529 |
| GWAS Ctlg | rs1956529 |
| GMAF | 0.4343 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20195514 ]
|
| Trait | Primary tooth development (number of teeth) |
| Title | Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy |
| Risk Allele | T |
| P-val | 3E-8 |
| Odds Ratio | 0.51 [NR] % variance explained |
