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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF10
(H207P)
Single nucleotide variant
(missense variant)
FGF10-related condition
+4 more
GBenign/Likely benign
FGF10
(V33I)
Single nucleotide variant
(missense variant)
FGF10-related condition
+3 more
GBenign/Likely benign