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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPC4
(A217V)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
STK26, TFDP3
+9 more
Copy number loss
Nystagmus 1, congenital, X-linked
+1 more
GPathogenic