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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KDM5C
Single nucleotide variant
(intron variant)
Syndromic X-linked intellectual disability Claes-Jensen type
GUncertain significance
KDM5C
(W467C +2 more)
Single nucleotide variant
(missense variant +1 more)
Syndromic X-linked intellectual disability Claes-Jensen type
GLikely pathogenic
KDM5C
(G462A +2 more)
Single nucleotide variant
(missense variant +1 more)
Syndromic X-linked intellectual disability Claes-Jensen type
GUncertain significance
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