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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD3
(P710fs +1 more)
Deletion
(frameshift variant)
Snijders Blok-Campeau syndrome
GUncertain significance
CHD3
(G786C +1 more)
Single nucleotide variant
(missense variant)
Snijders Blok-Campeau syndrome
GUncertain significance