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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCDC2, KAAG1
(A93D)
Single nucleotide variant
(missense variant)
Isolated neonatal sclerosing cholangitis
+2 more
GUncertain significance
DCDC2, KAAG1
(V51L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
DCDC2, KAAG1
(S42fs)
Microsatellite
(frameshift variant)
Dyslexia, susceptibility to, 2
+3 more
GPathogenic
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