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