rs1046934
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1046934(A;A) |
| Make rs1046934(A;C) |
| Make rs1046934(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 184054395 |
| Gene | TSEN15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1046934 |
| dbSNP (classic) | rs1046934 |
| ClinGen | rs1046934 |
| ebi | rs1046934 |
| HLI | rs1046934 |
| Exac | rs1046934 |
| Gnomad | rs1046934 |
| Varsome | rs1046934 |
| LitVar | rs1046934 |
| Map | rs1046934 |
| PheGenI | rs1046934 |
| Biobank | rs1046934 |
| 1000 genomes | rs1046934 |
| hgdp | rs1046934 |
| ensembl | rs1046934 |
| geneview | rs1046934 |
| scholar | rs1046934 |
| rs1046934 | |
| pharmgkb | rs1046934 |
| gwascentral | rs1046934 |
| openSNP | rs1046934 |
| 23andMe | rs1046934 |
| SNPshot | rs1046934 |
| SNPdbe | rs1046934 |
| MSV3d | rs1046934 |
| GWAS Ctlg | rs1046934 |
| GMAF | 0.3214 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 2E-31 |
| Odds Ratio | .04 [NR] unit decrease |
[PMID 19474294] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
[PMID 24944287] Genetic Variants Related to Height and Risk of Atrial Fibrillation: The Cardiovascular Health Study
