rs1052553, MAPT

N. diseases: 8
Disease: Essential Tremor ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
0.020 GeneticVariation BEFREE A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor. 27456607 2016
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
0.020 GeneticVariation BEFREE A meta-analysis of the H1/H2 tagging SNP rs1052553 in published data sets and the H1 haplotype with risk for ET in the current study was also performed and did not find evidence for association. 24372973 2014