rs11915082
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11915082(A;A) |
Make rs11915082(A;G) |
Make rs11915082(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 196082268 |
Gene | TFRC |
is a | snp |
is | mentioned by |
dbSNP | rs11915082 |
dbSNP (classic) | rs11915082 |
ClinGen | rs11915082 |
ebi | rs11915082 |
HLI | rs11915082 |
Exac | rs11915082 |
Gnomad | rs11915082 |
Varsome | rs11915082 |
LitVar | rs11915082 |
Map | rs11915082 |
PheGenI | rs11915082 |
Biobank | rs11915082 |
1000 genomes | rs11915082 |
hgdp | rs11915082 |
ensembl | rs11915082 |
geneview | rs11915082 |
scholar | rs11915082 |
rs11915082 | |
pharmgkb | rs11915082 |
gwascentral | rs11915082 |
openSNP | rs11915082 |
23andMe | rs11915082 |
SNPshot | rs11915082 |
SNPdbe | rs11915082 |
MSV3d | rs11915082 |
GWAS Ctlg | rs11915082 |
GMAF | 0.2328 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19862010![]() |
Trait | Mean corpuscular hemoglobin |
Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
Risk Allele | A |
P-val | 8E-13 |
Odds Ratio | 0 [0.003-0.005] pg increase |