Barely Significant
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Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.

PLoS One · 2008 · PMC2566815 · PMID 18941528

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highly significantno p-value reported
marginally significantno p-value reported
Linkage disequilibrium measures are highly significant between SNPs rs1327328 and rs7326018 and SNP rs4284505, located next to a cluster of microRNAs, and marginally significant with SNP rs9583760, located within LOC121727 (similar to Peroxisome assembly protein 12 (Peroxin-12) (Peroxisome assembly factor 3) (PAF-3)).

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