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indel associated_with SNV

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

Evidence (1 sources)

Annotation of functional variation in personal genomes using RegulomeDB. (2012) PMID:22955989 cited
these data would be inserted in the same manner as SNVs and are not distinguished as being of a different category
confidence: 0.90