rs1457451
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 |
Make rs1457451(A;A) |
Make rs1457451(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 65635244 |
Gene | LOC105369166 |
is a | snp |
is | mentioned by |
dbSNP | rs1457451 |
dbSNP (classic) | rs1457451 |
ClinGen | rs1457451 |
ebi | rs1457451 |
HLI | rs1457451 |
Exac | rs1457451 |
Gnomad | rs1457451 |
Varsome | rs1457451 |
LitVar | rs1457451 |
Map | rs1457451 |
PheGenI | rs1457451 |
Biobank | rs1457451 |
1000 genomes | rs1457451 |
hgdp | rs1457451 |
ensembl | rs1457451 |
geneview | rs1457451 |
scholar | rs1457451 |
rs1457451 | |
pharmgkb | rs1457451 |
gwascentral | rs1457451 |
openSNP | rs1457451 |
23andMe | rs1457451 |
SNPshot | rs1457451 |
SNPdbe | rs1457451 |
MSV3d | rs1457451 |
GWAS Ctlg | rs1457451 |
GMAF | 0.1414 |
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 | 0.000003 |
Odds Ratio | NR NR |