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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INTS1
Single nucleotide variant
(splice acceptor variant)
Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
+1 more
GLikely pathogenic
INTS1
(R1130C)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
+1 more
GUncertain significance
INTS1
(E930K)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
GUncertain significance
INTS1
(R77C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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