Normal allele: AA
The RIT2 rs12456492 polymorphism is associated with Parkinson's disease.
Polymorphism rs12456492 is related to topics like this:
Research and publications:
23635658 The RIT2 variant is not associated with Parkinson's disease in the Taiwanese population.
25457028 RIT2 polymorphism is associated with Parkinson's disease in the Han population.
25534083 RIT2 and STX1B polymorphisms are associated with Parkinson's disease.
25559334 Assessing the association of RIT2 rs12456492 with Parkinson's disease in mainland China.
26188085 RIT2 rs12456492 polymorphism and risk of Parkinson's disease: a meta-analysis.
27504496 Trans-pQTL study identifies immune crosstalk between Parkinson and Alzheimer loci.
27889863 Investigating the genetic association between RIT2 and Parkinson's disease in a Han population.
33987465 Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes.
34305570 pH-eQTL interaction at the Parkinson's disease risk locus RIT2-SYT4 in the substantia nigra.
35695987 Neurodegeneration-related gene polymorphisms are associated with Parkinson's disease risk.