rs10510146
From SNPedia
| Merged into | rs9422897 |
| Orientation | plus |
| Stabilized | plus |
| Make rs10510146(G;G) |
| Make rs10510146(G;T) |
| Make rs10510146(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 125607576 |
| Gene | TEX36 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10510146 |
| dbSNP (classic) | rs10510146 |
| ClinGen | rs10510146 |
| ebi | rs10510146 |
| HLI | rs10510146 |
| Exac | rs10510146 |
| Gnomad | rs10510146 |
| Varsome | rs10510146 |
| LitVar | rs10510146 |
| Map | rs10510146 |
| PheGenI | rs10510146 |
| Biobank | rs10510146 |
| 1000 genomes | rs10510146 |
| hgdp | rs10510146 |
| ensembl | rs10510146 |
| geneview | rs10510146 |
| scholar | rs10510146 |
| rs10510146 | |
| pharmgkb | rs10510146 |
| gwascentral | rs10510146 |
| openSNP | rs10510146 |
| 23andMe | rs10510146 |
| SNPshot | rs10510146 |
| SNPdbe | rs10510146 |
| MSV3d | rs10510146 |
| GWAS Ctlg | rs10510146 |
| Status | Merged into rs9422897 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20708005 ]
|
| Trait | |
| Title | Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease |
| Risk Allele | A |
| P-val | 0.000007 |
| Odds Ratio | 0.23 [NR] unit increase |
