Variant: rs6052751

present in Gene: RPS4XP2 present in Chromosome: 20 Position on Chromosome: 4664427 Alleles of this Variant: G/A;C

rs6052751 in RPS4XP2 gene and Prion Diseases PMID 22210626 2012 Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.