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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZMYND11
(D134H +13 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ZMYND11
(P112L +13 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ZMYND11
(R600W +15 more)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay
+4 more
GPathogenic/Likely pathogenic
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