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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRSS56
(R74fs)
Deletion
(frameshift variant)
Isolated microphthalmia 6
GPathogenic
PRSS56
(Q356fs +1 more)
Duplication
(frameshift variant)
PRSS56-related condition
+3 more
GPathogenic/Likely pathogenic
PRSS56
(L408V +1 more)
Single nucleotide variant
(missense variant)
Isolated microphthalmia 6
GUncertain significance
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