|
rs7605378
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Polymorphisms of the FONG (FTCDNL1) gene (rs7605378) were reported to be associated with the risk of osteoporosis in a Japanese population.
|
26492493 |
2015 |
|
rs7605378
|
|
|
0.830 |
GeneticVariation |
BEFREE |
We previously reported 2 osteoporosis-susceptibility genes--formiminotransferase N-terminal sub-domain containing gene (FONG) and thrombospondin, type 1, domain-containing 7A (THSD7A)--in which we identified two common single-nucleotide polymorphisms, rs7605378 (FONG) and rs12673692 (THSD7A).
|
23303384 |
2013 |
|
rs7605378
|
|
|
0.830 |
GeneticVariation |
GWASCAT |
Through these staged association studies followed by resequencing and linkage disequilibrium mapping, we identified a single nucleotide polymorphism (SNP), rs7605378 associated with osteoporosis.
|
21573128 |
2011 |
|
rs7605378
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Through these staged association studies followed by resequencing and linkage disequilibrium mapping, we identified a single nucleotide polymorphism (SNP), rs7605378 associated with osteoporosis.
|
21573128 |
2011 |
|
rs7605378
|
|
|
0.830 |
GeneticVariation |
GWASDB |
Through these staged association studies followed by resequencing and linkage disequilibrium mapping, we identified a single nucleotide polymorphism (SNP), rs7605378 associated with osteoporosis.
|
21573128 |
2011 |
|
rs2278729
|
|
|
0.810 |
GeneticVariation |
BEFREE |
All of the functional evidence suggested the important functional mechanisms underlying the associations of the 2 SNPs (rs2278729 and rs3736228) and 3 genes (RPL31, CPT1A and MTL5) with osteoporosis.
|
28369098 |
2017 |
|
rs2278729
|
|
A |
0.810 |
GeneticVariation |
GWASDB |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs2278729
|
|
A |
0.810 |
GeneticVariation |
GWASCAT |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs784288
|
|
A |
0.800 |
GeneticVariation |
GWASDB |
Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.
|
23349225 |
2013 |
|
rs784288
|
|
A |
0.800 |
GeneticVariation |
GWASCAT |
Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.
|
23349225 |
2013 |
|
rs12151790
|
|
A |
0.800 |
GeneticVariation |
GWASDB |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs12151790
|
|
A |
0.800 |
GeneticVariation |
GWASCAT |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs12808199
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs12808199
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs13182402
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis.
|
20072603 |
2010 |
|
rs13182402
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis.
|
20072603 |
2010 |
|
rs17184557
|
|
A |
0.800 |
GeneticVariation |
GWASDB |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs17184557
|
|
A |
0.800 |
GeneticVariation |
GWASCAT |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs2062375
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs2062375
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs494453
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs494453
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs7227401
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs7227401
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
|
20548944 |
2010 |
|
rs397514702
|
|
|
0.740 |
GeneticVariation |
BEFREE |
Cohort comprised mutation-positive (N = 13; age 17-76 years) and mutation-negative (N = 13; 16-77 years) subjects from two Finnish families with autosomal dominant WNT1 osteoporosis due to a heterozygous missense mutation c.652T>G (p.C218G) in WNT1.
|
31299386 |
2019 |