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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL25A1
(P506fs +1 more)
Deletion
(frameshift variant +1 more)
Fibrosis of extraocular muscles, congenital, 5
GPathogenic
COL25A1
(G502S +1 more)
Single nucleotide variant
(missense variant +1 more)
Fibrosis of extraocular muscles, congenital, 5
GUncertain significance