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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF9
Single nucleotide variant
(intron variant)
Multiple synostoses syndrome 3
+1 more
GBenign
FGF9
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
FGF9
Single nucleotide variant
(synonymous variant)
Multiple synostoses syndrome 3
+1 more
GBenign
FGF9
Single nucleotide variant
(3 prime UTR variant)
Multiple synostoses syndrome 3
+1 more
GBenign
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