Condition: Osteoporosis
rs13182402 in
ALDH7A1 gene and
Osteoporosis
PMID 20072603 2010 Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis.
rs2062375 in
COLEC10 gene and
Osteoporosis
PMID 20548944 2010 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
rs17184557 in
DOK6 gene and
Osteoporosis
PMID 20548944 2010 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
rs7605378 in
FTCDNL1 gene and
Osteoporosis
PMID 21573128 2011 Through these staged association studies followed by resequencing and linkage disequilibrium mapping, we identified a single nucleotide polymorphism (SNP), rs7605378 associated with osteoporosis.
rs494453 in
KRT18P57;RAP1A gene and
Osteoporosis
PMID 20548944 2010 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
rs784288 in
MECOM gene and
Osteoporosis
PMID 23349225 2013 Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.
rs7227401 in
OSBPL1A gene and
Osteoporosis
PMID 20548944 2010 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
rs11872467 in
RAB31 gene and
Osteoporosis
PMID 28580392 2016 A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women.
rs16965654 in
RPS16P8 gene and
Osteoporosis
PMID 20548944 2010 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
rs297325 in
SOX6 gene and
Osteoporosis
PMID 19714249 2009 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males.
rs12775980 in
SVIL gene and
Osteoporosis
PMID 28580392 2016 A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women.
rs2278729 in
TBC1D8 gene and
Osteoporosis
PMID 20548944 2010 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
rs397514702 in
WNT1;WNT10B gene and
Osteoporosis
PMID 23656646 2013 In 10 family members with dominantly inherited, early-onset osteoporosis, we identified a heterozygous missense mutation in WNT1, c.652T→G (p.Cys218Gly).
PMID 23499309 2013 Mutations in WNT1 cause different forms of bone fragility.