rs3018362 increases susceptibility to Osteoporotic fractures for carriers of the A allele [PMID 18445777]
related to Paget’s disease of bone 23andMe blog.
GWAS snp
|
PMID
|
[PMID 20436471]
|
Trait
|
Paget's disease
|
Title
|
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
|
Risk Allele
|
A
|
P-val
|
5E-13
|
Odds Ratio
|
1.52 [1.36-1.70]
|
GWAS snp
|
PMID
|
[PMID 21623375]
|
Trait
|
|
Title
|
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
|
Risk Allele
|
A
|
P-val
|
8E-21
|
Odds Ratio
|
1.4500 [1.34-1.56]
|
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