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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYOC
(Y497*)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
MYOC
Single nucleotide variant
(synonymous variant)
Glaucoma of childhood
GBenign
MYOC
Single nucleotide variant
(synonymous variant)
Glaucoma of childhood
GLikely benign
MYOC
(R76K)
Single nucleotide variant
(missense variant)
Glaucoma of childhood
GBenign
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