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SNV associated_with coding variant

Subject
SNV
Relation
associated_with
Object
coding variant
p-value
Evidence from: primary | all sources

Evidence (1 sources)

Annotation of functional variation in personal genomes using RegulomeDB. (2012) PMID:22955989 cited
Integration of all types of variants (SNVs, Indels, and SVs) with all types of noncoding and coding variants
confidence: 0.85