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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXE3, LINC01389
(D6N)
Single nucleotide variant
(missense variant)
Congenital primary aphakia
+4 more
GBenign/Likely benign
FOXE3, LINC01389
(P112S)
Single nucleotide variant
(missense variant)
Congenital primary aphakia
+2 more
GUncertain significance
FOXE3, LINC01389
Microsatellite
(inframe_insertion)
Congenital primary aphakia
+2 more
GUncertain significance
FOXE3, LINC01389
(G310D)
Single nucleotide variant
(missense variant)
not specified
+4 more
GBenign/Likely benign
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