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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSPAN2
(R118L +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
TSPAN2
Single nucleotide variant
(intron variant)
not provided
GBenign
AMPD1, AP4B1
+23 more
Duplication
RASopathy
GUncertain significance
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