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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL18A1
(S194L)
Single nucleotide variant
(missense variant +1 more)
Glaucoma, primary closed-angle
+3 more
GUncertain significance
COL18A1, SLC19A1
(A1333T +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
COL18A1, SLC19A1
(R1180Q +2 more)
Single nucleotide variant
(missense variant)
Knobloch syndrome
+2 more
GConflicting classifications of pathogenicity
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