rs12988804, LRP2

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.710 GeneticVariation BEFREE Variant rs12988804 in LRP2, the first example of a genome-wide significant association with relapse rate in MS, is replicated in an independent study. 29303040 2018
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.710 GeneticVariation GWASCAT In the pooled results, using these three unique longitudinal MS cohorts, we discovered one novel locus (<i>LRP2</i>; most significant single nucleotide polymorphism rs12988804) that reached genome-wide significance in predicting relapse risk (HR=2.18, p=3.30×10<sup>-8</sup>). 28739605 2017
Disease recurrence
CUI: C0679254
Disease: Disease recurrence
0.700 GeneticVariation GWASCAT Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis. 28739605 2017