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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NUP88
(P504S)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 4
GUncertain significance
NUP88
(L373F)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 4
+1 more
GUncertain significance
RTN4RL1, SCARF1
+115 more
Copy number gain
Chromosome 17P13.3, telomeric, duplication syndrome
GPathogenic
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