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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZMYND8
(S1028L +17 more)
Single nucleotide variant
(missense variant)
ZMYND8-related disorder
GLikely benign
ZMYND8
(A617S +11 more)
Single nucleotide variant
(missense variant)
ZMYND8-related disorder
GUncertain significance
ZMYND8
(S534F +5 more)
Single nucleotide variant
(missense variant +1 more)
ZMYND8-related disorder
GUncertain significance
ZMYND8
(T528P +5 more)
Single nucleotide variant
(missense variant +1 more)
ZMYND8-related disorder
GUncertain significance
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