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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPEF2
(S133N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
SPEF2
(P545S)
Single nucleotide variant
(missense variant)
Spermatogenic failure 43
+2 more
GLikely benign