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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SHMT2
(N73S +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
GUncertain significance
SHMT2
(A232V +2 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
GUncertain significance