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PPARG associated_with copy number variation

Subject
PPARG
Relation
associated_with
Object
copy number variation
p-value
—
Evidence from: primary | all sources

Evidence (1 sources)

Marker selection for genetic case-control association studies. (2009) PMID:19390530 cited
Useful features to look at are copy number variations (CNVs) ... displayed using the HapMap Genome Browser for PPARG.
confidence: 0.90