rs4353250
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4353250(C;C) |
Make rs4353250(C;T) |
Make rs4353250(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 18301970 |
Gene | HPS5 |
is a | snp |
is | mentioned by |
dbSNP | rs4353250 |
dbSNP (classic) | rs4353250 |
ClinGen | rs4353250 |
ebi | rs4353250 |
HLI | rs4353250 |
Exac | rs4353250 |
Gnomad | rs4353250 |
Varsome | rs4353250 |
LitVar | rs4353250 |
Map | rs4353250 |
PheGenI | rs4353250 |
Biobank | rs4353250 |
1000 genomes | rs4353250 |
hgdp | rs4353250 |
ensembl | rs4353250 |
geneview | rs4353250 |
scholar | rs4353250 |
rs4353250 | |
pharmgkb | rs4353250 |
gwascentral | rs4353250 |
openSNP | rs4353250 |
23andMe | rs4353250 |
SNPshot | rs4353250 |
SNPdbe | rs4353250 |
MSV3d | rs4353250 |
GWAS Ctlg | rs4353250 |
GMAF | 0.1938 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21124955] |
Trait | |
Title | Genome-Wide Association Study Identifies Two Novel Regions at 11p15.5-p13 and 1p31 with Major Impact on Acute-Phase Serum Amyloid A |
Risk Allele | T |
P-val | 2E-51 |
Odds Ratio | 0.2700 [0.23-0.31] unit increase |