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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SRGAP2
(P338S +1 more)
Single nucleotide variant
(missense variant)
SRGAP2-associated Neurodevelopmental Disorder
GUncertain significance
SRGAP2
(R235H)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance