rs5749446
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5749446(C;C) |
Make rs5749446(C;T) |
Make rs5749446(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 32484598 |
Gene | FBXO7 |
is a | snp |
is | mentioned by |
dbSNP | rs5749446 |
dbSNP (classic) | rs5749446 |
ClinGen | rs5749446 |
ebi | rs5749446 |
HLI | rs5749446 |
Exac | rs5749446 |
Gnomad | rs5749446 |
Varsome | rs5749446 |
LitVar | rs5749446 |
Map | rs5749446 |
PheGenI | rs5749446 |
Biobank | rs5749446 |
1000 genomes | rs5749446 |
hgdp | rs5749446 |
ensembl | rs5749446 |
geneview | rs5749446 |
scholar | rs5749446 |
rs5749446 | |
pharmgkb | rs5749446 |
gwascentral | rs5749446 |
openSNP | rs5749446 |
23andMe | rs5749446 |
SNPshot | rs5749446 |
SNPdbe | rs5749446 |
MSV3d | rs5749446 |
GWAS Ctlg | rs5749446 |
GMAF | 0.489 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23222517] |
Trait | Red blood cell traits |
Title | Seventy-five genetic loci influencing the human red blood cell. |
Risk Allele | T |
P-val | 3E-13 |
Odds Ratio | .01 [-0.00084-0.01484] unit increase |