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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPHB4
(P324H)
Single nucleotide variant
(missense variant)
Malignant neoplastic disease
GUncertain significance
LRP1B
Single nucleotide variant
(splice donor variant)
Malignant neoplastic disease
GUncertain significance
BRAF
(V600E +7 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
STier I - Strong
OOncogenic
PTPN11
(E76K +1 more)
Single nucleotide variant
(missense variant)
RASopathy
+3 more
GConflicting classifications of pathogenicity
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