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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT12
Deletion
(inframe_indel)
Corneal dystrophy, Meesmann, 1
GUncertain significance
KRT12
(L384P)
Single nucleotide variant
(missense variant)
Corneal dystrophy, Meesmann, 1
GUncertain significance