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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CBL, LOC130006895
Single nucleotide variant
(synonymous variant)
RASopathy
+3 more
GLikely benign
CBL, LOC130006895
(K6Q)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
+2 more
GUncertain significance
CBL, LOC130006895
(I26T)
Single nucleotide variant
(missense variant)
RASopathy
+1 more
GUncertain significance
CBL, LOC130006895
Microsatellite
(inframe_insertion)
not specified
+7 more
GBenign/Likely benign
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