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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VARS1
(F1072L)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy
+7 more
GConflicting classifications of pathogenicity
VARS1
(A22D)
Single nucleotide variant
(missense variant)
Intellectual disability
+5 more
GUncertain significance