| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (intron variant) | Intellectual disability, autosomal recessive 65 +1 more | GConflicting classifications of pathogenicity |
| | KDM5B, LOC129932249 (P68T) | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal recessive 65 +1 more | |
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