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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13L
(T867I)
Single nucleotide variant
(missense variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GLikely pathogenic
MED13L
(K250fs)
Deletion
(frameshift variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GPathogenic