Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1044032
rs1044032
0.020 GeneticVariation BEFREE The SNP rs1044032 (P = 6.42 × 10<sup>-5</sup>, OR = 0.80) was identified as significantly associated with PMOP. 29855663

2018

dbSNP: rs1044032
rs1044032
0.020 GeneticVariation BEFREE Based on the results of an in silico prediction of the protein's functional effect based on amino acid alterations and a sequence conservation evaluation of the amino acid residues at the positions of the nsSNPs among orthologues, we selected one nsSNP in the SQRDL gene (rs1044032, SQRDL I264T) as a meaningful genetic variant associated with postmenopausal osteoporosis. 26258864

2015