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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD4
(V1608I +2 more)
Single nucleotide variant
(missense variant)
Sifrim-Hitz-Weiss syndrome
GConflicting classifications of pathogenicity
CHD4
Single nucleotide variant
(synonymous variant)
Sifrim-Hitz-Weiss syndrome
GUncertain significance
CHD4
(N819K +2 more)
Single nucleotide variant
(missense variant)
Sifrim-Hitz-Weiss syndrome
GUncertain significance
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