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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL17A1
(S1381L)
Single nucleotide variant
(missense variant)
Epithelial recurrent erosion dystrophy
GUncertain significance
COL17A1
Single nucleotide variant
(intron variant)
Epithelial recurrent erosion dystrophy
GUncertain significance
COL17A1
(R688*)
Single nucleotide variant
(nonsense)
Epithelial recurrent erosion dystrophy
GPathogenic
COL17A1
(R154*)
Single nucleotide variant
(nonsense)
Epithelial recurrent erosion dystrophy
GPathogenic
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