rs29880
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs29880(A;A) |
Make rs29880(A;G) |
Make rs29880(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 40914882 |
is a | snp |
is | mentioned by |
dbSNP | rs29880 |
dbSNP (classic) | rs29880 |
ClinGen | rs29880 |
ebi | rs29880 |
HLI | rs29880 |
Exac | rs29880 |
Gnomad | rs29880 |
Varsome | rs29880 |
LitVar | rs29880 |
Map | rs29880 |
PheGenI | rs29880 |
Biobank | rs29880 |
1000 genomes | rs29880 |
hgdp | rs29880 |
ensembl | rs29880 |
geneview | rs29880 |
scholar | rs29880 |
rs29880 | |
pharmgkb | rs29880 |
gwascentral | rs29880 |
openSNP | rs29880 |
23andMe | rs29880 |
SNPshot | rs29880 |
SNPdbe | rs29880 |
MSV3d | rs29880 |
GWAS Ctlg | rs29880 |
GMAF | 0.1501 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19084217] |
Trait | Serum markers of iron status |
Title | Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | NR NR |