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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXE3, LINC01389
(M82V)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
FOXE3, LINC01389
(R90L)
Single nucleotide variant
(missense variant)
Congenital primary aphakia
+2 more
GUncertain significance
FOXE3, LINC01389
(S211*)
Single nucleotide variant
(nonsense)
Congenital primary aphakia
+1 more
GPathogenic/Likely pathogenic
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