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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13L
(Q1452fs)
Deletion
(frameshift variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GLikely pathogenic
MED13L
(I1338fs)
Deletion
(frameshift variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GPathogenic
MED13L
(R1342C)
Single nucleotide variant
(missense variant)
Cardiac anomalies - developmental delay - facial dysmorphism syndrome
GConflicting classifications of pathogenicity
MED13L
(P293L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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