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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRAS
(M189L)
Single nucleotide variant
(missense variant +1 more)
KRAS-related disorder
+2 more
GConflicting classifications of pathogenicity
KRAS
(V14I)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic
KRAS
(G13D)
Single nucleotide variant
(missense variant)
RASopathy
+6 more
GConflicting classifications of pathogenicity
KRAS
Single nucleotide variant
(synonymous variant)
RASopathy
GLikely benign
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