MAPT, microtubule associated protein tau, 4137

N. diseases: 469; N. variants: 292
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62063857
rs62063857
Entrez Id: 4137;246744
Gene Symbol: MAPT;STH
MAPT;STH
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation BEFREE The four previously reported Parkinson's disease (PD)-related single-nucleotide polymorphisms (SNPs) - rs1775143, rs823114, rs2071746 and rs62063857 - have rarely been studied in Chinese Han populations. 28535700 2017
dbSNP: rs62063857
rs62063857
Entrez Id: 4137;246744
Gene Symbol: MAPT;STH
MAPT;STH
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation BEFREE Consequently, the rs62063857 polymorphism of the saitohin gene is a genetic risk factor for Parkinson's disease. 25168738 2015
dbSNP: rs62063857
rs62063857
Entrez Id: 4137;246744
Gene Symbol: MAPT;STH
MAPT;STH
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs62063857
rs62063857
Entrez Id: 4137;246744
Gene Symbol: MAPT;STH
MAPT;STH
CUI: C0030567
Disease:
Parkinson Disease 		0.730 GeneticVariation BEFREE We identified a significant association between H1/H2 and risk of PD (rs1052553 OR: 1.43, CI: 1.23-1.64; rs62063857 OR: 1.45, CI: 1.27-1.67), but no effect of the H1-specific SNP rs242557 (OR: 0.92, CI: 0.82-1.03). 19912324 2010