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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCF20
(R1581fs)
Microsatellite
(frameshift variant)
Developmental delay with variable intellectual impairment and behavioral abnormalities
+1 more
GPathogenic
TCF20
(G1457R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
TCF20
(A1226G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
TCF20
(E1041Q)
Single nucleotide variant
(missense variant)
Developmental delay with variable intellectual impairment and behavioral abnormalities
+2 more
GUncertain significance
TCF20
(G49A)
Single nucleotide variant
(missense variant)
Developmental delay with variable intellectual impairment and behavioral abnormalities
GUncertain significance
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