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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZC4H2
(A177T +2 more)
Single nucleotide variant
(missense variant +1 more)
Wieacker-Wolff syndrome
GPathogenic
ZC4H2
(H193fs +2 more)
Deletion
(frameshift variant +1 more)
Wieacker-Wolff syndrome
GPathogenic
ZC4H2
(K164N +1 more)
Single nucleotide variant
(missense variant +2 more)
Wieacker-Wolff syndrome
GUncertain significance
ZC4H2
(Q34P +1 more)
Single nucleotide variant
(missense variant +1 more)
Wieacker-Wolff syndrome
GUncertain significance
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