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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRAS
(D153V)
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome
GPathogenic
KRAS
(C51S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KRAS
(Q22R)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic
KRAS
(G13D)
Single nucleotide variant
(missense variant)
RASopathy
+6 more
GPathogenic
OOncogenic
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