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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VARS1
(R1058Q)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy
+1 more
GLikely pathogenic
VARS1
(L16R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance