rs494453
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs494453(A;A) |
Make rs494453(A;G) |
Make rs494453(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 111649500 |
Gene | RAP1A |
is a | snp |
is | mentioned by |
dbSNP | rs494453 |
dbSNP (classic) | rs494453 |
ClinGen | rs494453 |
ebi | rs494453 |
HLI | rs494453 |
Exac | rs494453 |
Gnomad | rs494453 |
Varsome | rs494453 |
LitVar | rs494453 |
Map | rs494453 |
PheGenI | rs494453 |
Biobank | rs494453 |
1000 genomes | rs494453 |
hgdp | rs494453 |
ensembl | rs494453 |
geneview | rs494453 |
scholar | rs494453 |
rs494453 | |
pharmgkb | rs494453 |
gwascentral | rs494453 |
openSNP | rs494453 |
23andMe | rs494453 |
SNPshot | rs494453 |
SNPdbe | rs494453 |
MSV3d | rs494453 |
GWAS Ctlg | rs494453 |
GMAF | 0.4307 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20548944] |
Trait | Osteoporosis |
Title | An Integration of Genome-Wide Association Study and
Gene Expression Profiling to Prioritize the Discovery of Novel Susceptibility Loci for Osteoporosis-Related Traits |
Risk Allele | C |
P-val | 4E-8 |
Odds Ratio | None None |