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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD4
(V1006G +2 more)
Single nucleotide variant
(missense variant)
Sifrim-Hitz-Weiss syndrome
GConflicting classifications of pathogenicity
CHD4
(R800H +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance