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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF469
(R912fs)
Deletion
(frameshift variant)
Brittle cornea syndrome 1
GLikely pathogenic
ZNF469
(P2956T)
Single nucleotide variant
(missense variant)
Brittle cornea syndrome 1
+1 more
GConflicting classifications of pathogenicity