rs7155454
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7155454(A;A) |
Make rs7155454(A;G) |
Make rs7155454(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 65035521 |
Gene | CHURC1-FNTB, FNTB, MAX |
is a | snp |
is | mentioned by |
dbSNP | rs7155454 |
dbSNP (classic) | rs7155454 |
ClinGen | rs7155454 |
ebi | rs7155454 |
HLI | rs7155454 |
Exac | rs7155454 |
Gnomad | rs7155454 |
Varsome | rs7155454 |
LitVar | rs7155454 |
Map | rs7155454 |
PheGenI | rs7155454 |
Biobank | rs7155454 |
1000 genomes | rs7155454 |
hgdp | rs7155454 |
ensembl | rs7155454 |
geneview | rs7155454 |
scholar | rs7155454 |
rs7155454 | |
pharmgkb | rs7155454 |
gwascentral | rs7155454 |
openSNP | rs7155454 |
23andMe | rs7155454 |
SNPshot | rs7155454 |
SNPdbe | rs7155454 |
MSV3d | rs7155454 |
GWAS Ctlg | rs7155454 |
GMAF | 0.388 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23222517] |
Trait | Red blood cell traits |
Title | Seventy-five genetic loci influencing the human red blood cell. |
Risk Allele | A |
P-val | 2E-12 |
Odds Ratio | .00 [-0.00584-0.00984] unit increase |