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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DYRK1A
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
DYRK1A
(A679P +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+3 more
GBenign/Likely benign