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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAPRIN1
(V175L)
Single nucleotide variant
(missense variant)
CAPRIN1-related disorder
GUncertain significance
CAPRIN1
(T478A)
Single nucleotide variant
(missense variant)
CAPRIN1-related disorder
GUncertain significance