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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED12
(R206G)
Single nucleotide variant
(missense variant)
FG syndrome
GUncertain significance
LOC126863275, MED12
(T459I)
Single nucleotide variant
(missense variant)
FG syndrome
GUncertain significance