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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KDM1A
(D181H)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
KDM1A
(A589T +3 more)
Single nucleotide variant
(missense variant)
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome
GUncertain significance
KDM1A
(A620T +3 more)
Single nucleotide variant
(missense variant)
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome
GUncertain significance
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