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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGFR3
(R248C)
Single nucleotide variant
(missense variant +1 more)
FGFR3-related disorder
+31 more
GPathogenic
FGFR3
(G380R +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+18 more
GPathogenic