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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGFR2
(G156P +3 more)
Inversion
(missense variant +2 more)
Crouzon syndrome
GLikely pathogenic
FGFR2
Insertion
Acrocephalosyndactyly type I
GLikely pathogenic