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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DYRK1A
(I152fs +2 more)
Deletion
(frameshift variant)
DYRK1A-related intellectual disability syndrome
+1 more
GPathogenic
DYRK1A
(L241P +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DYRK1A
(F308S +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely pathogenic
DYRK1A
(P582T)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GBenign/Likely benign
DYRK1A
(N634S +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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