rs1055129
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1055129(C;C) |
| Make rs1055129(C;T) |
| Make rs1055129(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 75876867 |
| Gene | TRIM47 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1055129 |
| dbSNP (classic) | rs1055129 |
| ClinGen | rs1055129 |
| ebi | rs1055129 |
| HLI | rs1055129 |
| Exac | rs1055129 |
| Gnomad | rs1055129 |
| Varsome | rs1055129 |
| LitVar | rs1055129 |
| Map | rs1055129 |
| PheGenI | rs1055129 |
| Biobank | rs1055129 |
| 1000 genomes | rs1055129 |
| hgdp | rs1055129 |
| ensembl | rs1055129 |
| geneview | rs1055129 |
| scholar | rs1055129 |
| rs1055129 | |
| pharmgkb | rs1055129 |
| gwascentral | rs1055129 |
| openSNP | rs1055129 |
| 23andMe | rs1055129 |
| SNPshot | rs1055129 |
| SNPdbe | rs1055129 |
| MSV3d | rs1055129 |
| GWAS Ctlg | rs1055129 |
| GMAF | 0.4008 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21681796 ]
|
| Trait | |
| Title | Genome-wide association studies of cerebral white matter lesion burden: The CHARGE consortium. |
| Risk Allele | G |
| P-val | 3E-11 |
| Odds Ratio | None None |
