1000 Genomes Project associated_with missense variants

Subject: 1000 Genomes Project
Relation: associated_with
Object: missense variants
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations. (2015) PMID:26394715 cited

We then benchmarked the extraction of nonsynonymous variants from 100 randomly selected genes.

confidence: 0.85