rs9525625
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9525625(C;C) |
Make rs9525625(C;T) |
Make rs9525625(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 42443894 |
Gene | LOC105370177 |
is a | snp |
is | mentioned by |
dbSNP | rs9525625 |
dbSNP (classic) | rs9525625 |
ClinGen | rs9525625 |
ebi | rs9525625 |
HLI | rs9525625 |
Exac | rs9525625 |
Gnomad | rs9525625 |
Varsome | rs9525625 |
LitVar | rs9525625 |
Map | rs9525625 |
PheGenI | rs9525625 |
Biobank | rs9525625 |
1000 genomes | rs9525625 |
hgdp | rs9525625 |
ensembl | rs9525625 |
geneview | rs9525625 |
scholar | rs9525625 |
rs9525625 | |
pharmgkb | rs9525625 |
gwascentral | rs9525625 |
openSNP | rs9525625 |
23andMe | rs9525625 |
SNPshot | rs9525625 |
SNPdbe | rs9525625 |
MSV3d | rs9525625 |
GWAS Ctlg | rs9525625 |
GMAF | 0.3742 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Rs9525625 | |
---|---|
PubMed | [PMID 18445777] |
Affy Probeset | SNP_A-2226987 |
Affy Orientation | same |
On GW 5.0 | |
Alleles A/B | C/T |
Ancestral | T |
Population | Caucasian |
Allele | C |
Case Freq. | |
Control Freq. | |
Odds Ratio Het | |
Odds Ratio Hom | |
Odds Ratio All | - |
Disease | Bone mineral density, lower (BMD-L) |
rs9525625 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mineral density variations, lower for carriers of the C allele [PMID 18445777]