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de novo variant associated_with rare disease

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

Evidence (1 sources)

The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019) PMID:31802016 cited
the loss-of-function variant frequency spectrum ... providing unique advantages for the identification of genes associated with both rare ... diseases
confidence: 0.90