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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDST, FLG2
(S319fs)
Microsatellite
(frameshift variant)
not provided
GLikely pathogenic
CCDST, FLG2
(S211*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic