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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF14
(C81* +8 more)
Single nucleotide variant
(nonsense)
Spinocerebellar ataxia type 27
GUncertain significance
FGF14
(P24L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance