rs12808199
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12808199(A;A) |
Make rs12808199(A;G) |
Make rs12808199(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 39306409 |
is a | snp |
is | mentioned by |
dbSNP | rs12808199 |
dbSNP (classic) | rs12808199 |
ClinGen | rs12808199 |
ebi | rs12808199 |
HLI | rs12808199 |
Exac | rs12808199 |
Gnomad | rs12808199 |
Varsome | rs12808199 |
LitVar | rs12808199 |
Map | rs12808199 |
PheGenI | rs12808199 |
Biobank | rs12808199 |
1000 genomes | rs12808199 |
hgdp | rs12808199 |
ensembl | rs12808199 |
geneview | rs12808199 |
scholar | rs12808199 |
rs12808199 | |
pharmgkb | rs12808199 |
gwascentral | rs12808199 |
openSNP | rs12808199 |
23andMe | rs12808199 |
SNPshot | rs12808199 |
SNPdbe | rs12808199 |
MSV3d | rs12808199 |
GWAS Ctlg | rs12808199 |
GMAF | 0.4582 |
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 | G |
P-val | 9E-7 |
Odds Ratio | 0.21 [NR] g/cm2 decrease |