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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFAP91
(Q419* +3 more)
Single nucleotide variant
(nonsense)
Spermatogenic failure 51
GLikely pathogenic
CFAP91, LOC129937328
(D42H)
Single nucleotide variant
(synonymous variant +2 more)
Spermatogenic failure 51
+1 more
GPathogenic
CFAP91
Single nucleotide variant
(splice donor variant)
Male infertility with teratozoospermia due to single gene mutation
+1 more
GPathogenic
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