[PMID 17357082] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

rs2283792

Parent Gene: MAPK1

Importance: 4
Less common allele: T = 46%
More common allele: G = 54%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Multiple Sclerosis

The C allele of rs2283792 is reported to be associated with Multiple Sclerosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Multiple sclerosis.