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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGFR3
(P62S)
Single nucleotide variant
(missense variant +1 more)
FGFR3-related disorder
+14 more
GUncertain significance
FGFR3
(R248C)
Single nucleotide variant
(missense variant +1 more)
Epidermal nevus
+31 more
GPathogenic