rs1867082
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1867082(C;C) |
| Make rs1867082(C;T) |
| Make rs1867082(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 85270825 |
| Gene | RNU3P3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1867082 |
| dbSNP (classic) | rs1867082 |
| ClinGen | rs1867082 |
| ebi | rs1867082 |
| HLI | rs1867082 |
| Exac | rs1867082 |
| Gnomad | rs1867082 |
| Varsome | rs1867082 |
| LitVar | rs1867082 |
| Map | rs1867082 |
| PheGenI | rs1867082 |
| Biobank | rs1867082 |
| 1000 genomes | rs1867082 |
| hgdp | rs1867082 |
| ensembl | rs1867082 |
| geneview | rs1867082 |
| scholar | rs1867082 |
| rs1867082 | |
| pharmgkb | rs1867082 |
| gwascentral | rs1867082 |
| openSNP | rs1867082 |
| 23andMe | rs1867082 |
| SNPshot | rs1867082 |
| SNPdbe | rs1867082 |
| MSV3d | rs1867082 |
| GWAS Ctlg | rs1867082 |
| GMAF | 0.4587 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23534349 ]
|
| Trait | QRS duration |
| Title | Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans. |
| Risk Allele | A |
| P-val | 1E-6 |
| Odds Ratio | 2.82 [NR] ms increase |
[PMID 17903299] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.
