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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIGF, CRIPT
Deletion
Rothmund-Thomson syndrome, type 3
GPathogenic
CRIPT
(C3Y)
Single nucleotide variant
(missense variant)
Rothmund-Thomson syndrome, type 3
GLikely pathogenic
CRIPT
Single nucleotide variant
(intron variant)
Rothmund-Thomson syndrome, type 3
GUncertain significance
CRIPT
Copy number loss
Rothmund-Thomson syndrome, type 3
GPathogenic
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