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SNP associated_with de novo variant

Subject
SNP
Relation
associated_with
Object
de novo variant
p-value
Evidence from: primary | all sources

Evidence (1 sources)

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. (2013) PMID:24076603 cited
Wells in which SNP regions were amplified by qPCR were assumed to contain DNA fragments spanning the amplified SNP and the de novo deletion.
confidence: 0.96