The OLR1 rs1050283 SNP likely acts as a risk factor for sporadic AD.The presence of at least one C allele is associated with a decreased expression of OLR1 mRNA in the absence of hsa-miR369-3p de-regulation,suggesting that the presence of the polymorphic allele influences the binding of hsa-miR369-3p to its 3’UTR consensus sequence.
NSDNA: The Nervous System Disease NcRNAome Atlas
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