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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRDL1
(K230M +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TMEM31, TMEM35A
+488 more
Copy number gain
not provided
GPathogenic
AWAT2, BCLAF3
+568 more
Copy number gain
not provided
GUncertain significance
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