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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13L
(Q1473*)
Single nucleotide variant
(nonsense)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GPathogenic
MED13L
(S773fs)
Deletion
(frameshift variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GPathogenic