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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STRN4, FKRP
+1 more
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance
AP2S1, ARHGAP35
+33 more
Copy number gain
not provided
GPathogenic