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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED12
(M243T)
Single nucleotide variant
(missense variant)
FG syndrome 1
GUncertain significance
MED12
(A1383T)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
MED12
(T1945S)
Single nucleotide variant
(missense variant)
FG syndrome
+1 more
GUncertain significance
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