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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FSIP2
Deletion
(nonsense)
Spermatogenic failure 34
GLikely pathogenic
FSIP2-AS1, FSIP2
Duplication
(non-coding transcript variant +1 more)
Spermatogenic failure 34
+2 more
GConflicting classifications of pathogenicity