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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFAP221
Single nucleotide variant
(splice donor variant)
Primary ciliary dyskinesia
GLikely pathogenic
CFAP221
(L768fs)
Deletion
(frameshift variant +1 more)
Primary ciliary dyskinesia
GLikely pathogenic