rs10067427
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs10067427(A;G) |
| Make rs10067427(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 100006343 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10067427 |
| dbSNP (classic) | rs10067427 |
| ClinGen | rs10067427 |
| ebi | rs10067427 |
| HLI | rs10067427 |
| Exac | rs10067427 |
| Gnomad | rs10067427 |
| Varsome | rs10067427 |
| LitVar | rs10067427 |
| Map | rs10067427 |
| PheGenI | rs10067427 |
| Biobank | rs10067427 |
| 1000 genomes | rs10067427 |
| hgdp | rs10067427 |
| ensembl | rs10067427 |
| geneview | rs10067427 |
| scholar | rs10067427 |
| rs10067427 | |
| pharmgkb | rs10067427 |
| gwascentral | rs10067427 |
| openSNP | rs10067427 |
| 23andMe | rs10067427 |
| SNPshot | rs10067427 |
| SNPdbe | rs10067427 |
| MSV3d | rs10067427 |
| GWAS Ctlg | rs10067427 |
| GMAF | 0.4206 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | G |
| P-val | 0.000005 |
| Odds Ratio | 0.75 [NR] unit increase |
