rs6752877
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6752877(G;G) |
Make rs6752877(G;T) |
Make rs6752877(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 54434432 |
Gene | LOC102724072 |
is a | snp |
is | mentioned by |
dbSNP | rs6752877 |
dbSNP (classic) | rs6752877 |
ClinGen | rs6752877 |
ebi | rs6752877 |
HLI | rs6752877 |
Exac | rs6752877 |
Gnomad | rs6752877 |
Varsome | rs6752877 |
LitVar | rs6752877 |
Map | rs6752877 |
PheGenI | rs6752877 |
Biobank | rs6752877 |
1000 genomes | rs6752877 |
hgdp | rs6752877 |
ensembl | rs6752877 |
geneview | rs6752877 |
scholar | rs6752877 |
rs6752877 | |
pharmgkb | rs6752877 |
gwascentral | rs6752877 |
openSNP | rs6752877 |
23andMe | rs6752877 |
SNPshot | rs6752877 |
SNPdbe | rs6752877 |
MSV3d | rs6752877 |
GWAS Ctlg | rs6752877 |
GMAF | 0.1763 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
Rs6752877 | |
---|---|
PubMed | [PMID 18445777] |
Affy Probeset | SNP_A-2263153 |
Affy Orientation | reverse |
On GW 5.0 | |
Alleles A/B | A/C |
Ancestral | T |
Population | Caucasian |
Allele | T |
Case Freq. | |
Control Freq. | |
Odds Ratio Het | |
Odds Ratio Hom | |
Odds Ratio All | 1.11 |
Disease | Osteoporotic fractures (OP-F) |
rs6752877 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.11 times for carriers of the T allele [PMID 18445777]