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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXP1
(R514H +4 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
FOXP1
Single nucleotide variant
(intron variant)
Intellectual disability-severe speech delay-mild dysmorphism syndrome
GUncertain significance
FOXP1
(Q60del)
Microsatellite
(inframe_deletion +2 more)
Intellectual disability-severe speech delay-mild dysmorphism syndrome
+1 more
GUncertain significance
FOXP1
Single nucleotide variant
(intron variant)
Intellectual disability-severe speech delay-mild dysmorphism syndrome
GUncertain significance
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