Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10410544
rs10410544
0.060 GeneticVariation BEFREE There is an association between the <i>SIRT2-C/T</i> genotype (rs10410544) (50.92%) and AD susceptibility in the <i>APOEε4</i>-negative population (<i>SIRT2-C/C</i>, 34.72%; <i>SIRT2-T/T</i> 14.36%). 30871086

2019

dbSNP: rs10410544
rs10410544
0.060 GeneticVariation BEFREE A number of genetic variants have previously been identified and associated with the risk of Alzheimer's disease (AD), including rs10838725 in CELF1, rs28834970 in PTK2B, rs17125944 in FERMT2, and rs10410544 in SIRT2 based on genome-wide association studies. 30144538

2018

dbSNP: rs10410544
rs10410544
0.060 GeneticVariation BEFREE SIRT2 polymorphism rs10410544 is associated with Alzheimer's disease in a Han Chinese population. 24139700

2014

dbSNP: rs10410544
rs10410544
0.060 GeneticVariation BEFREE The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease: a meta-analysis. 24497179

2014

dbSNP: rs10410544
rs10410544
0.060 GeneticVariation BEFREE We failed to find any association between rs10410544 genotype and AD in the two samples. 23712749

2013

dbSNP: rs10410544
rs10410544
0.060 GeneticVariation BEFREE The SIRT2 rs10410544 T allele deserves further investigation as a novel minor genetic risk factor for AD in the APOE ε4-negative Caucasian population. 22651940

2013