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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EIF3F
(F232V)
Single nucleotide variant
(missense variant)
Intellectual disability
+6 more
GPathogenic/Likely pathogenic
BPTF
(M1676V +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
GUncertain significance