rs10838681
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10838681(A;A) |
| Make rs10838681(A;G) |
| Make rs10838681(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 47253513 |
| Gene | NR1H3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10838681 |
| dbSNP (classic) | rs10838681 |
| ClinGen | rs10838681 |
| ebi | rs10838681 |
| HLI | rs10838681 |
| Exac | rs10838681 |
| Gnomad | rs10838681 |
| Varsome | rs10838681 |
| LitVar | rs10838681 |
| Map | rs10838681 |
| PheGenI | rs10838681 |
| Biobank | rs10838681 |
| 1000 genomes | rs10838681 |
| hgdp | rs10838681 |
| ensembl | rs10838681 |
| geneview | rs10838681 |
| scholar | rs10838681 |
| rs10838681 | |
| pharmgkb | rs10838681 |
| gwascentral | rs10838681 |
| openSNP | rs10838681 |
| 23andMe | rs10838681 |
| SNPshot | rs10838681 |
| SNPdbe | rs10838681 |
| MSV3d | rs10838681 |
| GWAS Ctlg | rs10838681 |
| GMAF | 0.4284 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22399527 ]
|
| Trait | |
| Title | Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. |
| Risk Allele | G |
| P-val | 1E-9 |
| Odds Ratio | 0.0800 None |
[PMID 17357082] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
