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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DYNC1H1
(R1804Q)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
DYNC1H1
(E4056K)
Single nucleotide variant
(missense variant)
Global developmental delay
GUncertain significance