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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD7
(I843V)
Single nucleotide variant
(missense variant +1 more)
CHARGE syndrome
GLikely benign
CHD7
(R2400Q)
Single nucleotide variant
(missense variant +1 more)
CHARGE syndrome
GBenign
CHD7
(A2925V +1 more)
Single nucleotide variant
(missense variant)
CHARGE syndrome
GUncertain significance
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