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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKL5, RS1
(I194fs)
Duplication
(frameshift variant +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic
CDKL5, RS1
(Q913H)
Single nucleotide variant
(missense variant +1 more)
CDKL5 disorder
GLikely benign
CDKL5, RS1
(R102Q)
Single nucleotide variant
(missense variant +1 more)
Retinal dystrophy
+2 more
GPathogenic
CDKL5, RS1
(W96R)
Single nucleotide variant
(missense variant +1 more)
Retinal dystrophy
+2 more
GPathogenic
CDKL5, RS1
(E72Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic
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