U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13L
(E1908Q)
Single nucleotide variant
(missense variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GLikely pathogenic
MED13L
(R1342C)
Single nucleotide variant
(missense variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GConflicting classifications of pathogenicity