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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP1B1, LOC128772254
(D430E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CYP1B1
(V320L)
Single nucleotide variant
(missense variant)
Congenital glaucoma
+5 more
GConflicting classifications of pathogenicity
CYP1B1
(L107V)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
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