rs17277546
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs17277546(A;A) |
| Make rs17277546(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 99891948 |
| Gene | TRIM4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17277546 |
| dbSNP (classic) | rs17277546 |
| ClinGen | rs17277546 |
| ebi | rs17277546 |
| HLI | rs17277546 |
| Exac | rs17277546 |
| Gnomad | rs17277546 |
| Varsome | rs17277546 |
| LitVar | rs17277546 |
| Map | rs17277546 |
| PheGenI | rs17277546 |
| Biobank | rs17277546 |
| 1000 genomes | rs17277546 |
| hgdp | rs17277546 |
| ensembl | rs17277546 |
| geneview | rs17277546 |
| scholar | rs17277546 |
| rs17277546 | |
| pharmgkb | rs17277546 |
| gwascentral | rs17277546 |
| openSNP | rs17277546 |
| 23andMe | rs17277546 |
| SNPshot | rs17277546 |
| SNPdbe | rs17277546 |
| MSV3d | rs17277546 |
| GWAS Ctlg | rs17277546 |
| GMAF | 0.02663 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21533175 |
| Trait | |
| Title | Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. |
| Risk Allele | A |
| P-val | 2E-11 |
| Odds Ratio | 0.1100 [0.07-0.15] umol/L decrease |
[PMID 28146470
] Rare and low-frequency coding variants alter human adult height.
| GWAS snp | |
|---|---|
| PMID | [PMID 21886157 |
| Trait | |
| Title | Human metabolic individuality in biomedical and pharmaceutical research. |
| Risk Allele | A |
| P-val | 9E-40 |
| Odds Ratio | 0.4760 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 7
- 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
