rs4988321, LRP5

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
0.040 GeneticVariation BEFREE In contrast, there was an increased value of OR in heterozygotes for rs4988321, both in patients with osteopenia (OR = 1.47) and in those with osteoporosis (OR = 1.33). 29963786 2019
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
0.040 GeneticVariation BEFREE The less common Val667Met polymorphism showed no association with osteoporosis. 24885293 2014
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
0.040 GeneticVariation BEFREE In this study were determined the allelic and genotypic frequencies of four polymorphic markers (C/T rs3736228, G/A rs4988321, T/C rs627174 and T/C rs901824) in the low-density lipoprotein receptor-related protein 5 gene (LRP5) and their association with osteoporosis in 100 pos-menopausal osteoporotic Mexican women and their controls, using real time-PCR and TaqMan probes. 23242660 2013
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
0.040 GeneticVariation BEFREE Genotypes and haplotypes were based on LRP5 missense substitutions in exons 9 (c.2047G > A, p.V667M) and 18 (c.4037C > T, p.A1330V), and their association with osteoporosis evaluated after adjustment for multiple clinical and environmental variables using logistic regression. 16168727 2005