rs6079395
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6079395(A;A) |
| Make rs6079395(A;G) |
| Make rs6079395(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 14347253 |
| Gene | MACROD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6079395 |
| dbSNP (classic) | rs6079395 |
| ClinGen | rs6079395 |
| ebi | rs6079395 |
| HLI | rs6079395 |
| Exac | rs6079395 |
| Gnomad | rs6079395 |
| Varsome | rs6079395 |
| LitVar | rs6079395 |
| Map | rs6079395 |
| PheGenI | rs6079395 |
| Biobank | rs6079395 |
| 1000 genomes | rs6079395 |
| hgdp | rs6079395 |
| ensembl | rs6079395 |
| geneview | rs6079395 |
| scholar | rs6079395 |
| rs6079395 | |
| pharmgkb | rs6079395 |
| gwascentral | rs6079395 |
| openSNP | rs6079395 |
| 23andMe | rs6079395 |
| SNPshot | rs6079395 |
| SNPdbe | rs6079395 |
| MSV3d | rs6079395 |
| GWAS Ctlg | rs6079395 |
| GMAF | 0.404 |
| 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 | A |
| P-val | 0.000007 |
| Odds Ratio | 0.92 [NR] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 20
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
