SNP information rs112176450
Normal allele: GG
A rare EIF4G1 mutation causes an 8-fold increase in Parkinson's disease.
Polymorphism rs112176450 is related to topics like this:
A disorder that progresses gradually within the nervous system is known as Parkinson's disease. It...
Research and publications:
21907011 Translation initiator EIF4G1 mutations in familial Parkinson disease.
23408866 Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.
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