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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD7
(Y835fs)
Deletion
(frameshift variant +1 more)
not provided
+1 more
GPathogenic
CHD7
(R1054Q)
Single nucleotide variant
(missense variant +1 more)
CHARGE association
+2 more
GConflicting classifications of pathogenicity
CHD7
(W1786R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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