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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFAP58
(Q436* +1 more)
Single nucleotide variant
(nonsense)
Spermatogenic failure 49
GLikely pathogenic
CFAP58
(R698*)
Single nucleotide variant
(nonsense)
Spermatogenic failure 49
GPathogenic