rs1461496
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1461496(A;A) |
Make rs1461496(A;G) |
Make rs1461496(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 123058916 |
Gene | HSPA8, SNORD14C, SNORD14D, SNORD14E |
is a | snp |
is | mentioned by |
dbSNP | rs1461496 |
dbSNP (classic) | rs1461496 |
ClinGen | rs1461496 |
ebi | rs1461496 |
HLI | rs1461496 |
Exac | rs1461496 |
Gnomad | rs1461496 |
Varsome | rs1461496 |
LitVar | rs1461496 |
Map | rs1461496 |
PheGenI | rs1461496 |
Biobank | rs1461496 |
1000 genomes | rs1461496 |
hgdp | rs1461496 |
ensembl | rs1461496 |
geneview | rs1461496 |
scholar | rs1461496 |
rs1461496 | |
pharmgkb | rs1461496 |
gwascentral | rs1461496 |
openSNP | rs1461496 |
23andMe | rs1461496 |
SNPshot | rs1461496 |
SNPdbe | rs1461496 |
MSV3d | rs1461496 |
GWAS Ctlg | rs1461496 |
GMAF | 0.3159 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20300519] Genetic Variations in HSPA8 Gene Associated with Coronary Heart Disease Risk in a Chinese Population
[PMID 22370858] Pharmacogenetics of asthma controller treatment.