SNV associated_with noncoding variant

Subject: SNV
Relation: associated_with
Object: noncoding variant
p-value: —

Evidence from: primary | all sources

Evidence (2 sources)

Annotation of functional variation in personal genomes using RegulomeDB. (2012) PMID:22955989 cited

We find that a majority of variants are noncoding

confidence: 0.92

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